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ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Ambroxol Hydrochloride Tablets Each uncotaed coated tablet contains:
Ambroxol Hydrochloride 30 mg.
Desloratadine Tablets Each film-coated tablet contains:
Desloratadine 5 mg
Excipients
Colour: Lake of Indigo Carmine & Titanium
Dioxide I.P.
q.s.
Doxophylline Sustained Release Tablets Each uncoated sustained release tablet contains:
Doxophylline 400/800 mg
Doxophylline 400mg Tablet Each uncoated tablet contains
Doxophylline 400 mg
Fexofenadine Tablets Each Film coated tablet conatins:
Fexofenadine HCl
Colour: Yellow Iron Oxide & Titanium Dioxide
120/180 mg
Guaiphenesin, Bromhexine HCl,
Phenylpropanolamione HCL &
Chlorpheniramine Maleate
Tablets Each uncoated tablet contains
Guaiphenesin IP 100 mg
Bromhexine Hydrochloride IP 8 mg
Phenylpropanolamine Hydrochloride USP 5 mg
Chlorpheniramine Maleate IP 2 mg
Paracetamol IP 500 mg
Levocetrizine Dihydrochloride Tablets Each film coated tablet contains:
Levocetrizine Dihydrochloride Colour:
Titanium Dioxide
5 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Levocetrizine, Ambroxol, and Phenyl Epherine
HCl Tablets Each film coated tablet contains:
Levocetrizine Dihydrochloride 5 mg
Ambroxol Hydrochloride BP 60 mg
Phenyl Epherine HCl IP
Colour: Erthrosine
5 mg
Montelukast, Levocetirizine and Acebrophylline
(SR) Tablets Each film coated bilayered tablet contains :
Montelukast Sodium IP
equivalent to Montelukast 10 mg
Levocetirizine Hydrochloride IP
Acebrophylline
5 mg
( sustained release form) 200 mg
Excipients
Approved Colours used
q.s
Montelukast Sodium & Levocetirizine HCl Tablets Each uncoated tablet contains
Montelukast Sodium eq. to Montelukast 10 mg
Levocetirizine Hydrochloride IP
Colour: Tartrazine Lake & Titanium Dioxide IP
5 mg
Montelukast Sodium & Levocetirizine HCl Tablets Each dispersible tablet contains
Montelukast Sodium eq. to Montelukast 4 mg
Levocetirizine Hydrochloride IP
Colours : Sunset yellow lake & Titanium Dioxide
IP
2.5 mg
Montelukast Sodium Tablets Each uncoated tablet contains:
Montelukast Sodium IP eq. to Montelukast
Colour: Tartrazine
10 mg
Paracetamol,Phenylephrine,Cetirizine HCl &
Caffiene Tablets Each uncoated tablet contains:-
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Paracetamol I.P. 500 mg
Phenylephrine 5 mg
Cetirizine HCl B.P. 5 mg
Caffiene (ANHY.) I.P. 30 mg
Prochlorperazine Maleate and Paracetamol Tablets Each uncoated tablet contains:
Prochlorperazine Maleate I.P. 5 mg.
Paracetamol I.P. 500 mg.
Paracetamol, Guaiphenesin, Ambroxol
Hydrochloride, Phenylephrine
Tablets Hydrochloride and Chlorpheniramine Maleate
Tablets
Each film coated tablet contains
Paracetamol IP 325 mg
Guaiphenesin IP 100 mg
Ambroxol Hydrochloride IP 30 mg
Phenylephrine Hydrochloride IP 10 mg
Chlorpheniramine Maleate IP 2 mg
Excipients q.s.
Ambroxol Hydrochloride Syrup Each 5ml Contains:
Ambroxol Hydrochloride BP 30 mg
Acebrophylline Syrup Each 5ml contains:
Acebrophylline
Colour: Sunset Yellow FCF
50 mg
Ambroxol Syrup Each 5ml contains:
Ambroxol 30 mg
Ambroxol HCl, Terbutaline and Guaiphenesin Syrup Each teaspoonful (5ml) contains:
Ambroxol Hydrochloride BP 15 mg
Terbutaline Sulphate IP 2.5 mg
Guaiphenesin IP 50 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Flavoured Syrup base q.s.
Ambroxol HBr and Terbutaline Syrup Each 5ml contains:
Ambroxol Hydrochloride BP 15 mg
Terbutaline Sulphate IP 2.5 mg
Flavoured Syrupy base
Colour: Tartrazine & Sunset yellow FCF
q.s.
Ambroxol Hcl, Terbutaline Sulphate &
Guaiphenesin Syrup Each 5ml contains
Ambroxol Hydrochloride IP 15 mg
Terbutaline Sulphate IP 1.25 mg
Guaiphenesin IP 50 mg
Mentholated Flavoured Syrupy base Colour:
Sunset Yellow FCF.
q.s.
Ambroxol HCl, Terbutaline Sulphate &
Guaiphenesin Syrup Each 5ml contains
Ambroxol Hydrochloride IP 30 mg
Terbutaline Sulphate IP 1.25 mg
Guaiphenesin IP 50 mg
Menthol Flavoured base
Colour: Sunset Yellow FCF.
q.s.
Ambroxol Hcl,Levosalbutamol and
Guaiphenesin Syrup Each 5ml contains
Ambroxol Hydrochloride IP 7.5 mg
Guaiphenesin IP 12.50 mg
Levosalbutamol 0.25 mg
Ambroxol and cetrizine Syrup Each 5 ml. contains:
Ambroxol Hydrochloride B.P. 30 mg.
Cetirizine Hydrochloride B.P. Colour:Sunset
yellow FCF
2.5 mg.
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Ambroxol Hcl , Levosalbutamol and
Guaiphenesin Syrup Each 5ml contains
Ambroxol Hydrochloride IP 15 mg
Guaiphenesin IP 50 mg
Levosalbutamol 0.5 mg
Bromhexine, Phenylephrine and Guaiphenesin Syrup Each 5ml contains:
Bromhexine Hydrochloride IP 4 mg
Guaiphenesin IP 50 mg
Phenylephrine Hydrochloride IP 2.5 mg
Cetirizine Syrup Each 5 ml contains:
Cetirizine 5 mg
Levocetirizine and Ambroxol Syrup Levocetirizine 2.5 / 5 mg.
Ambroxol Hydrochloride 30 mg.
Levocetirizine and Montelukast HCl Syrup Each 5ml contains
Levocetirizine Hydrochloride IP 2.5 mg
Montelukast Sodium IP eq. to Montelukast Colour
: Sunset yellow FCF
4 mg
CPM, Ammonium Chloride and sodium citrate Syrup Each 5ml Contains:-
Chlorampheniramine Maleate IP 4 mg
Ammonium Chloride IP 125 mg
Sodium Citrate IP 55 mg
Menthol Ip
Colour- Carmoisine
1 mg
Cyproheptadine HCl and Tricholine citrate Syrup Each 5ml (one teaspoonful) contains:
Cyproheptadine Hydrochloride IP 2 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Tricholine Citrate 275 mg
Sorbitol (70%) (Non Crystalline) IP Colour:
Caramal IP
q.s.
Chlorpheniramine and Phenyephrine Drops Each ml contains
Chlorpheniramine Maleate 1 mg
Phenylephrine Hcl 2.5 mg
Chlorpheniramine & Phenylephrine Maleate Drops Each ml contains:
Phenylephrine Hydrochloride USP 2.5 mg
Chlorpheniramine Maleate IP Colour:
Sunset Yellow FCF
2 mg
Chlorpheniramine Maleate, Ammonium
Chloride & Sodium Citrate Drops Each 5ml (one teaspoonful) contains:
Chlorpheniramine Maleate IP 2.5 mg
Ammonium Chloride IP 125 mg
Sodium Citrate IP 55 mg
Mentholated Flavoured Syrupy base Colour:
Sunset Yellow FCF
q.s.
CPM, Ammonium Chloride and sodium citrate Each 5ml Contains:-
Chlorampheniramine Maleate IP 4 mg
Ammonium Chloride IP 125 mg
Sodium Citrate IP 55 mg
Menthol Ip
Colour- Carmoisine
1 mg
Chlorpheniramine Maleate & Phenylephrine
Hydrochloride
Each 5ml (one teaspoonful) contains:
Chlorpheniramine Maleate IP 2 mg
Phenylephrine Hydrochloride IP Colour:
Sunset Yellow FCF
5 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Chlorpheniramine, Paracetamol &
Phenylepherine Syrup Each 5ml (one teaspoonful) contains:
Paracetamol IP 125 mg
Phenylepherine 5 mg
Chlorpheniramine Maleate IP
Colour: Sunset Yellow FCF
2 mg
Dextromethorphan HBr and Phenylepherine Syrup Each teaspoonful (5ml) contains:
Dextromethorphan Hydrobromide IP 10 mg
Phenylpropanolamine Hydrochloride USP 5 mg
Flavoured Syrup base
Colour: Tartrazine
q.s.
Dextromethorphan & Guaphenesin Syrup Each 5Ml Contains:-
Dextromethorphan HBR IP 15 mg
Guaiphenesin IP 100 mg
Sorbitol IP 0.33 mg
Excipients & Flavours q.s
Dextromethorphan HBr, Bromhexine Hcl &
Ammonium Chloride
Each 5ml (one teaspoonful) contains:
Dextromethorphan Hydrobromide IP 5 mg
Bromhexine Hydrochloride IP 4 mg
Ammonium Chloride 50 mg
Mentholated Flavoured Syrupy base
Colour: Brilliant Blue & Tartrazine
q.s
Dextromethorphan Hydrobromide, Triprolidine
& Phenylepherine Syrup Each 5 ml contains:
Dextromethorphan Hydrobromide IP 10 mg
Triprolidine Hydrochloride IP 1.25 mg
Phenylephrine 2 mg
Menthol IP 1.5 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Colour - Ponceau 4R
Dextromethorphan HBr and Phenylepherine Syrup Each teaspoonful (5ml) contains:
Dextromethorphan Hydrobromide IP 10 mg
Phenylpropanolamine Hydrochloride USP 5 mg
Flavoured Syrup base Colour:
Tartrazine
q.s.
Dextromethrophan, Guaiphenesin,
Phenylepherine and CPM Syrup Each 5Ml contains :
Guaiphenesin IP 100 mg
Dextromethorphan HBr IP 10 mg
Phenylepherine 5 mg
Chlorampheniramine Maleate IP 4 mg
Flavoured Syrup Base Colour-
Ponceau 4R
q.s
Dextromethorphan and Chlorpheniramine
Maleate Syrup Each 5 ml contains:
Dextromethorphan Hydrobromide IP 10 mg
Chlorpheniramine Maleate IP 4 mg
Flavoured Base
Colours - Sunset Yellow FCF & Caramel IP
q.s.
Dextromethorphan HBr, Phenylephrine HCl &
Chlorpheniramine Maleate
Each 5ml (one teaspoonful) contains:
Dextromethorphan Hydrobromide IP 10 mg
Phenylephrine Hydrochloride IP 5 mg
Chlorpheniramine Maleate IP 2 mg
Flavoured Syrupy base Colour:
Brilliant Blue
q.s
Doxophylline Syrup Each 5ml contains
Doxophylline 100 mg
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Colour: Sunset Yellow FCF
Fexofenadine oral Suspenion Each 5 ml contains
Fexofenadine 30 mg
Paracetamol, Phenylephrine HCl &
Chlorpheniramine Maleate
Each 5ml (one teaspoonful) contains:
Paracetamol IP 125 mg
Phenylephrine Hydrochloride USP 2.5 mg
Chlorpheniramine Maleate IP Colour:
Sunset Yellow FCF
1 mg
Phenylephrine HCl & Chlorpheniramine
Maleate Drops Each 1ml contains:
Phenylephrine Hydrochloride USP 2.5 mg
Chlorpheniramine Maleate IP Colour:
Sunset Yellow FCF
2 mg
Paracetamol, Phenylephrine & Cetirizine Oral Suspension Each 5ml contains:
Paracetamol IP 250 mg.
Phenylephrine HCl IP 5 mg.
Cetirizine Hydrochloride BP
Colour: Erythrosine & Sunset Yellow
2.5 mg.
Phenylephrine HCl, Chlorpheniramine Maleate,
Paracetamol & Sodium Citrate Suspension Each 5ml contains:
Phenylephrine Hydrochloride IP 5 mg
Chlorpheniramine Maleate IP 0.5 mg
Paracetamol IP 125 mg
Sodium Citrate
In a Mentholated flavoured syrupy base
60 mg
Salbutamol Syrup Each 5ml contains
ANTI-ALLERGIC / ANTI-COLD PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Salbutamol 2 mg
Terbutaline Sulphate with Etophylline Syrup Each 5ml contains:
Terbutaline Sulphate IP 1.25 mg
Etophylline IP
Colour: Sunset Yellow FCF
50 mg
Acebrophylline 100 mg Capsules Each hard gelatin capsule contains:
Acebrophylline 100 mg
Excipients
Approved colours used in capsule shell
q.s.
Ranitidine Oral Solution USP Oral Solution Each Sml contains:
Ranitidine Hyrochloride IP
Equivalent to Ranitidine
Flavoured Syrupy base 75 mg
Approved Colours used q.s
ANTI-BACTERIAL / ANTI-INFECTIVE
PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Azithromycin Tablets Each uncoated tablet contains:
Azithromycin U.S.P. (as dihydrate) equ. to
Azithromycin (anhydrous) 250/500 mg
Ciprofloxacin Hydrochloride and Tinidazole Tablets Each film coated tablet contains:
Ciprofloxacin Hydrochloride I.P.
equivalent to Ciprofloxacin 500 mg.
Tinidazole IP
Colour: Sunset Yellow FCF
600 mg.
Ciprofloxacin Hydrochloride and Ornidazole Tablets Each film coated tablet contains: Ciprofloxacin Hydrochloride I.P.
equivalent to Ciprofloxacin 500 mg.
Ornidazole
Colour: Sunset Yellow FCF
500 mg.
Furazolidone Tablets Each uncoated tablet contains:
Furazolidine I.P. 100 mg
Griseofluvin Tablets Each film coated tablet contains:
Griseofluvin
Colour: Titanium Dioxide I.P.
250/375/500 mg
Levofloxacin Tablets Each film coated tablet contains:
Levofloxacin Hemihydrate
eq. to Levofloxacin
Colour: Yellow Oxide of Iron, Red Oxide of Iron & Titanium
Dioxide IP
250/500/750 mg.
Linezolid Hcl Tablets Each film coated tablet contains:
Linezolid Hcl 600 mg
Minocycline Hydrochloride Tablets Each Film coated Tablet Contains:
ANTI-BACTERIAL / ANTI-INFECTIVE
PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Minocycline Hydrochloride USP Equivalent
to Minocycline
50 /100 mg
Excipients Colour : Titanium Dioxide & Sunset yellow
q.s.
Norfloxacin Tablets Each film coated tablet contains
Norfloxacin Hcl 200/400/800 mg
Nitrofurantoin Tablets Each film coated tablet contains:
Nitrofurantoin
Colour: Titanium Dioxide I.P.
100 mg
Nitrofurantoin Sustained Realese Tablets 100
mg Tablets Each film coated sustained release tablet contains:
Nitrofurantoin IP 100 mg
Excipients q.s.
Nitrofurantoin Modified Release Tablets Each modified release tablet contains:
Nitrofurantoin Colour: Titanium Dioxide I.P.
100 mg
Ofloxacin Tablets Each Film coated tablet contains:
Ofloxacin USP 100/200/400 mg
Prulifloxacin Tablets Each film coated tablet contains:
Prulifloxacin
Colour: Yellow oxide of Iron & Titanium Dioxide I.P.
600 mg
Roxithromycin Tablets Each film coated tablet
Roxithromycin B.P. 150/300 mg
Terbinafine Tablets Each Un-coated tablet contains: Terbinafine
Hydrochloride
ANTI-BACTERIAL / ANTI-INFECTIVE
PRODUCT RANGE TYPE LABEL CLAIMS
STRENGTH
eq. to Terbinafine 250 mg
Azithromycin Suspension Each 5 ml contains Azithromycin U.S.P. (as dihydrate) equ. to azithromycin
(anhydrous) USP
100 mg
Flavoures syrupy base q.s.
Azithromycin Suspension Each 5 ml contains
Azithromycin U.S.P. (as dihydrate) equ. to azithromycin
(anhydrous) USP
200 mg
Flavoures syrupy base q.s.
Ofloxacin Suspension Each 5 ml. contains:
Ofoxacin U.S.P. 50 mg
Excipients
Colour: Quinoline yellow & Sunset yellow FCF
q.s.
Doxycycline Capsules Each capsule contains
Doxycycline HCl eqv. To doxycyline 100 mg
Norfloxacin and Tinidazole Tablets Each film coated tablet contains:
Norfloxacin IP 400 mg
Tinidazole IP
Excipients
Approved colours used
600 mg
Saccharomyces Boulardii 250 MG Sachet Each sachet contains:
Lyophiilised Saccharomyces Boulardii 250 mg
Excipients q.s
ANTI-EMETICS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Betahistine Dihydrochloride Tablets Each Uncoated tablet cointains:
Betahistine Dihydrochloride 8 mg
Excipients q.s.
Betahistine Dihydrochloride Tablets Each Uncoated tablet cointains:
Betahistine Dihydrochloride 16 mg
Excipients q.s.
Betahistine Dihydrochloride Tablets Each Uncoated tablet cointains:
Betahistine Dihydrochloride 24 mg
Excipients q.s.
Ondansetron Tablets Each uncoated dispersible tablet contains:
Ondansetron HCl U.S.P. eq. to Ondansetron 4 /8 mg
Prochlorperazine Maleate Mouth Dissolving Tablets Each uncoated tablet contains :
Prochlorperazine maleate IP 5 mg
Excipients q.s.
Ondansetron Syrup Each 5 ml contains:
Ondansetron HCl U.S.P equ to Ondansetron 2 mg
Flavoured Syrup base
Colour : Ponceau 4 R
q.s.
ANTI-HELMINTHIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Albendazole Tablets Each uncoated tablet contains
Albendazole (micronised) 400 mg
Ivermectin Tablets Each Uncoated dispersible tablets contains:
Ivermectin 3 /6/12 mg
Excipients q.s.
Levamisole Tablets IP Tablets Each uncoated tablet contains:
Levamizole (as levamizole HCl IP) 150 mg
Albendazole Suspension Each 5ml contains:
Albendazole IP
Colour : Sunset Yellow FCF
200 mg
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Aceclofenac SR and Pregabalin SR Tablets Each bilayered sustained release tablet contains :
Aceclofenac I.P 200 mg
Pregabalin I.P 150 mg
Excipients
Approved colours used
q.s
Aceclofenac SR and Pregabalin SR Tablets Each bilayered sustained release tablet contains :
Aceclofenac I.P 200 mg
Pregabalin I.P 75 mg
Excipients
Approved colours used
q.s
Aceclofenac dispersible Tablets Each film uncoated dispersible tablet contains:
Aceclofenac B.P with
Betacyclodextrin
100 mg
Aceclofenac Tablets Each film-coated tablet contains:
Aceclofenac B.P.
Colour: Titanium Dioxide IP
100 mg
Aceclofenac Tablets Each Sustained Release tablet contains:
Aceclofenac B.P.
Colour: Ponceau 4R
200 mg
Aceclofenac & Paracetamol Tablets Each uncoated tablet contains:
Aceclofenac B.P. 100 mg
Paracetamol I.P. 500 mg
Aceclofenac & Paracetamol Tablets Each Uncoated tablet contains:
Aceclofenac I.P. 100 mg
Paracetamol I.P. 325 mg
Aceclofenac and Thiocolchicoside Tablets Each film coated tablet contains:
Aceclofenac IP 100 mg
Thiocolchicoside 4 mg
Excipients q.s.
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Colour: Quinoline Yellow WS
Aceclofenac and Thiocolchicoside Tablets Each film coated tablet contains:
Aceclofenac IP 100 mg
Thiocolchicoside 8 mg
Excipients
Colour: Quinoline Yellow WS & Titanium Dioxide IP
q.s.
Diclofenac Sodium and Thiocolchicoside Tablets Each film coated tablet contains:
Diclofenac Sodium IP 50 mg
Thiocolchicoside
Colour: Ponceau 4R
4 mg
Diclofenac Sodium and Thiocolchicoside Tablets Each film coated tablet contains:
Diclofenac Sodium IP 50 mg
Thiocolchicoside
Colour: Ponceau 4R
8 mg
Deflazacort Tablets Each film coated tablet contains
Deflazacort
Colour: Approved colour used
6 /24/30 mg
Diclofenac Pottasium & Paracetamol Tablets Each Un-coated dispersible tablet contains:
Diclofenac Pottasium 50 mg
Paracetamol I.P.
Colour: Tartrazine
500 mg
Diclofenac Sodium Tablets Each enteric coated tablet contains:
Diclofenac Sodium IP
Colour: Titanium Dioxide IP
50 mg
Diclofenac Sodium Tablets Each film coated sustained release tablet contains:
Diclofenac Sodium IP
Colour: Titanium Dioxide IP
75 /150 mg
Etodolac Tablets Each film coated tablet contains:
Etodolac USP/IP 200/300/400 mg
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Excipients
Colour:Titanium Dioxide I.P.
q.s.
Etodolac Extended Release Tablets Each film coated extended release tablet contains:
Etodolac USP 400/600 mg
Excipients
Colour:Titanium Dioxide I.P.
q.s.
Etodolac & Paracetamol Tablets Each film coated tablet contains:
Etodolac IP 400 mg
Paracetamol IP 500 mg
Excipients
Colours: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Etodolac & Paracetamol Tablets Each film coated bilayered tablet contains:
Etodolac IP 400 mg
Paracetamol IP 500 mg
Excipients
Colours: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Etodolac and Thiocolchicoside Tablets Each film coated tablet contains:
Etodolac IP 400 mg
Thiocolchicoside IP
Colours: Ferric Oxide Red USP NF & Titanium Dioxide IP
4 /8 mg
Etoricoxib and Thiocolchicoside Tablets Each film coated tablet contains:
Etoricoxib 60 mg
Thiocolchicoside IP 4 mg
Etoricoxib tablets 90mg Tablets Each film coated tablet contains:
Etoricoxib 90 mg
Etoricoxib tablets 60mg Tablets Each film coated tablet contains:
Etoricoxib 60 mg
Etoricoxib and Paracetamol tablets Each film coated tablet contains:
Etoricoxib 60 mg
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Paracetamol IP 325 mg
Nimesulide Tablets Each uncoated flavoured dispersible tablet contains:
Nimesulide B.P. 100 mg.
Excepients q.s.
Nimesulide Tablets Each uncoated tablet contains:
Nimesulide B.P.
Colour: Tartrazine
200 mg.
Nabumetone Tablets Each film coated tablet contains:
Nabumetone USP
Colour: Titanium Dioxide I.P.
1000 mg
Nabumetone & Paracetamol Tablets Each film coated tablet contains:
Nabumetone USP 500 mg
Paracetamol IP
Colour: Ferric Oxide Yellow USNF
500 mg
Paracetamol Tablets Each tablet contains:
Paracetamol I.P. 250/500/650 mg
Piroxicam Dispersible Tablets Each uncoated dispersible tablet contains:
Piroxicam IP (In β - Cyclodextrin)
Colours: Lake of Sunset Yellow FCF
10 mg
Paracetamol Tablets Each uncoated tablet contains:
Paracetamol I.P. 650 mg
Thiocolchicoside, Aceclofenac and Paracetamol Tablets Each film coated tablet contains :
Thiocolchicoside IP 4 mg
Aceclofenac IP 100 mg
Paracetamol IP 325 mg
Excipients
Approved Colours used
q.s
Thiocolchicoside, Aceclofenac and Paracetamol Tablets Each film coated tablet contains :
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Thiocolchicoside IP 8 mg
Aceclofenac IP 100 mg
Paracetamol IP 325 mg
Excipients
Approved Colours used
q.s
Tramadol Hydrochloride Dispersible Tablets Each uncoated dispersible tablet contains:
Tramadol Hydrochloride 37.5/50 mg.
Excipients q.s.
Tramadol Hydrochloride Dispersible Tablets Each uncoated sustained release tablet contains:
Tramadol Hydrochloride 50 /100 mg.
Excipients q.s.
Tramadol & Acetaminophen Tablets Each uncoated tablet contains:
Tramadol Hydrochloride B.P. 37.5 mg.
Acetaminophen I.P.
Colour :Tartrazine
325 mg.
Tranexamic & Mefenamic Tablets Each Film coated Tablet Contains:
Tranexamic Acid B.P. 500 mg
Mefenamic Acid I.P.
Colour: Quinoline Yellow
250 mg
Tranexamic & Mefenamic Tablets Each Film coated Tablet Contains:
Tranexamic Acid B.P. 250 mg
Mefenamic Acid I.P.
Colour: Quinoline Yellow
250 mg
Tranexamic Acid Tablets Each Film Coated tablet contains:
Tranexamic Acid B.P.
Colour: Titanium Dioxide
250/500 mg.
Trypsin, Bromelain, Rutoside Trihydrate &
Diclofenac Sodium Tablets
Each enteric coated tablet contains :
Trypsin B.P 48 mg
Bromelain 90 mg
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Rutoside Trihydrate B.P 100 mg
Diclofenac Sodium I.P 50 mg
Excipients
Approved colours used
q.s
Trypsin -Chymotrypsin with Paracetamol and
Aceclofenac Tablets Each film coated tablet contains :
Aceclofenac I.P 100 mg
Paracetamol I.P
50.000 units Armour units enzymatic activity
(Supplied by a purified concentrate which has specific Trypsin
& Chymotrypsin activity in a ratio of approximately six to one )
( As enteric coated granules )
325 mg
Excipients
Approved colours used
q.s
Acetaminophen Oral Susp. USP Suspension Each ml contains
Paracetamol IP
Colour:Sunset Yellow FCF.
100 mg
Deflazacort Suspension Each 5 ml contains:
Deflazacort 6 mg
Flavoured Syrupy Base
Colour - Quinoline Yellow
q.s.
Nimesulide Suspension Each 5ml (one teaspoonful) contains:
Nimesulide B.P.
in a flavoured syrupy base
Colour : Quinoline Yellow WS
50 mg
Promethazine and Paracetamol Suspension Each 5ml Contains:
Promethazine HCl IP 2.5 mg
Paracetamol IP 125 mg
Oxaceprol Capsules Each hard gelatin Capsule contains
Oxaceprol . 200 mg
Excipients q.s
ANTI-INFLAMATORY ANALGESIC PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Approved Colours used in Capsule shell
Thiocolchicoside Capsules Each hard gelatin capsule contains:
Thiocolchicoside
Approved colours used in capsule shells
4 mg
Thiocolchicoside Capsules Each hard gelatin capsule contains:
Thiocolchicoside
Approved colours used in capsule shells
8 mg
Tapentadol Tablets 50 mg Tablets Each film coated tablet contains :
Tapentadol Hydrochloride IP equivalent to Tapentadol 100 mg
Excipients
Approved colours used
q.s.
ANTI-MALARIALS PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Artesunate + Amodiaquine Tablets Each tablet contains
Artesunate 50 mg
Amodiaquine 153 mg
Artesunate +
Sulfadoxine+Pyrimethamine Tablets Each tablet contains
Artesunate 50 mg
Sulfadoxine 1000 mg
Pyrimethamine 50 mg
Atovaquone & Proguanil Tablets Each tablet contains
Atovaquone 250 mg
Proguanil 100 mg
Artesunate & Chloroquine Tablets Each tablet contains
Artesunate 50 mg
Chloroquine 250 mg
Artemether & Lumefantrine Tablets Each tablet contains
Artemether 20 /40/80 mg
Lumefantrine 120/240/480 mg
Hydroxychloroquine Sulfate Tablets Each film coated tablet contains
Hydroxychloroquine Sulfate USP Colour:
Titanium Dioxide IP
200 mg
ANTI-SPASMODICS PRODUCT
RANGE
TYPE LABEL CLAIMS STRENGTH
Drotaverine Hydrochloride Tablets Each uncoated tablet contains:
Drotaverine Hydrochloride 40 /80mg
Hyoscine butyl Bromide Tablets Each film coated tablet contains
Hyoscine Butyl Bromide 10 mg
Hyoscine Hydro Bromide Tablets Each film coated tablet contains
Hyoscine Hydro Bromide 10 mg
ANTI-VIRALS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Acyclovir Tablets Each uncoated tablet contains:
Acyclovir BP 200 / 400/800 mg
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Atenolol and Chlorthalidone Tablets Each tablet contains
Atenolol 25 /50 mg
Chlorthalidone IP 12.5 mg
Aspirin Tablets Each enteric coated tablet contains
Acetylsalicylic acid Colour : Titanium Dioxide IP
75/150/300 mg
Amlodipine Besylate Tablets Each uncoated tablet contains:
Amlodipine Besylate equivalent to
Amlodipine
Colour: Yellow Oxide of Iron
5 /10 mg.
Amlodipine & Atenolol Tablets Each uncoated tablet contains:
Amlodipine Besylate equivalent to
Amlodipine 5 mg.
Atenolol IP Colour: Lake of Sunset Yellow
50 mg
Cilnidipine and Metoprolol Succinate ER Tablets Each film coated bilayered tablet contains :
Cilnidipine 10 mg
Metoprolol Succinate USP 23.75 mg
equivalent to metoprolol tartrate (
in extended release form )
25 mg
Excipients Approved Colours used
q.s
Cilnidipine and Metoprolol Succinate ER Tablets Each film coated bilayered tablet contains :
Cilnidipine 10 mg
Metoprolol Succinate USP 47.5 mg
equivalent to metoprolol tartrate (
in extended release form )
50 mg
Excipients q.s
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Approved Colours used
Cilnidipine and Nebivolol Tablets Each film coated Bilayered tablet contains : Nebivolol
Hydrochloride IP
equivalent to Nebivolol 2.5 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
Cilnidipine and Nebivolol Tablets Each film coated Bilayered tablet contains : Nebivolol
Hydrochloride IP
equivalent to Nebivolol 5 mg
Cilnidipine 10 mg
Excipients Approved Colours used
q.s
Cilnidipine Tablets Each film coated tablet contains:
Cilnidipine
Colour : Titanium Dioxide IP
5 /10/20 mg
Chlorthalidone Tablets Each uncoated tablet contains
Chlorthalidone IP 6.25/12.5/25/50/100 mg
Excipients q.s.
Dronedarone HCL Tablets Each tablet contains
Dronedarone HCL 400 mg
Digoxin Tablets Each uncoated tablet contains:
Digoxin
Colour: Titanium Dioxide I.P.
0.25 mg
Diltiazem Tablets Each film coated tablet contains
Diltiazem IP Colour: Red Oxide of Iron & Titanium Dioxide IP
30 /60 mg
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Diltiazem Sustained Release Tablets Each film coated sustained release tablet contains
Diltiazem IP
Colou: Red Oxide of Iron & Titanium Dioxide IP
90 /120 mg
Etamsylate Tablets Each Uncoated tablet contains:
Etamsylate BP Colour: Iron Oxide Red
250/500 mg
Flunarizine Dihydrochloride Tablets Each uncoated tablet contains
Flunarizine Dihydrochloride BP eq. to Flunarizine 10 mg
Felodipine Tablets Each tablet contains
Felodipine 2.5/5 /10mg
Hydrochlorothiazide & Losartan Potassium Tablets Each uncoated tablet contains:
Hydrochorothiazide 12.5
Losartan Potassium USP 20 mg.
Hydrochlorothiazide Tablets Each uncoated tablet contains
Hydrochlorothiazide 25 mg
Isoxsuprine Hydrochloride Tablets Each uncoated tablet contains:
Isoxsuprine Hydrochloride I.P. 10 mg
Isoxsuprine Hydrochloride Tablets Each uncoated sustain release tablet contains:
Isoxsuprine Hydrochloride I.P. 40 mg
Losartan Pottasium Tablets Each film coated tabelt contains
Losartan Pottasium Colour: Sunset Yellow Lake
20 /40 mg
Lornoxicam and Paracetamol Tablets Each film coated tablet contains
Lornoxicam 4 /8mg
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Paracetamol IP 325/500 mg
Excipients
Colours: Yellow Oxide of Iron and Titanium Dioxide IP
q.s.
Lornoxicam and Thiocolchicoside Tablets Each film coated tablet contains:
Lornoxicam 4 /8 mg
Thiocolchicoside
Colour: Lake of Quinoline Yellow & Titanium
Dioxide IP
4 /8 mg
Metoprolol Succinate Extended Release Tablets USP
Tablets Each film coated Extended release tablet contains
Metoprolol Succinate USP 23.75 mg
Equivalent to Metoprolol Tartrate 25 mg
Metoprolol Succinate USP 47.50 mg
Equivalent to Metoprolol Tartrate 50 mg
Metoprolol Succinate USP 95 mg
Equivalent to Metoprolol Tartrate Colours:
Approved colours used
100 mg
Metoprolol Succinate ER & Telmisartan Tablets Each film coated bilayered tablet contains:
Metoprolol Succinate USP eq. to Metoprolol Tartrate 25 /50mg
Telmisartan IP Colour: Tartrazine
40 mg
Nebivolol and Chlorthalidone Tablets Each uncoated tablet contains : Nebivolol
Hydrochloride IP
equivalent to Nebivolol 5 mg
Chlorthalidone IP Excipients 12.5 mg
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Nebivolol Hydrochloride Tablets Each uncoated tablet contains
Nebivolol Hydrochloride eq. to Nebivolol 2.5/5 mg
Nebivolol +HCTZ Tablets Each tablet contains
Nebivolol 5 mg
Hydrochlorothiazode 12.5 mg
Olmesartan Medoxomil Tablets Each film coated bilayered tablet contains:
Olmesartan Medoxomil
Colour: Sunset Yellow Lake
20 /40 mg
Olmesartan Medoxomil & Metoprolol
Succinate ER
Tablets Each film coated bilayered tablet contains:
Metoprolol Succinate USP
eq. to Metoprolol Tartrate (as extended release) 25 mg
Olmesartan Medoxomil
Colour: Sunset Yellow Lake
20 mg
Olmesartan Medoxomil & Metoprolol
Succinate ER
Tablets Each film coated bilayered tablet contains:
Metoprolol Succinate USP
eq. to Metoprolol Tartrate (as extended release) 50 mg
Olmesartan Medoxomil
Colours: Sunset Yellow & Tartrazine
20 mg
Olmesartan Medoxomil and Cilnidipine Tablets Each film coated tablet contains
Olmesaratan Medoxomil BP 20 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
Olmesartan Medoxomil and Cilnidipine Tablets Olmesaratan Medoxomil BP 40 mg
Cilnidipine 10 mg
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Excipients
Approved Colours used
q.s
Prasugrel Hydrochloride Tablets Each film coated tablet contains:
Prasugrel Hydrochloride eq. to Prasugrel
Colour: Approved colour used
5 /10 mg
Propanalol Tablets Each uncoated tablet contains
Propanalol HCl 10/20/40/80 mg
Ranolazine Sustained Release Tablets Each uncoated sustained release tablet contains
Ranolazine 500/1000 mg
Ranolazine Tablets Each uncoated sustained release tablet contains
Ranolazine 1000 mg
S(-)Amlodipine & Losartan Potassium Tablets Each uncoated tablet contains: S(-)Amlodipine Besilate equivalent to
S(-)Amlodipine 2.5 mg.
Losartan Potassium USP Colour: Lake of Quinoline Yellow
50 mg.
S(-)Amlodipine Besilate Tablets Each uncoated tablet contains:
S(-)Amlodipine Besilate equivalent to
S(-)Amlodipine Colour: Yellow Oxide of Iron
1.25/2.5 mg.
S (-) Atenolol Tablets Each uncoated tablet contains:
S (-) Atenolol 12.5/25/50 mg
S (-) Atenolol & Hydrochlorothiazide Tablets Each uncoated tablet contains:
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
S (-) Atenolol 25 mg
Hydrochlorothiazide IP
Colour: Lake of Sunset Yellow
12.5 mg
Telmisartan Tablets Each uncoated tablet contains:
Telmisartan 20 /40/80 mg
Telmisartan & Hydrochlorothiazide Tablets Each uncoated tablet contains:
Telmisartan 40 mg
Hydrochlorothiazide 12.5 mg
Telmisartan & Amlodipine Tablets Each uncoated tablet contains:
Telmisartan B.P. 40 mg
Amlodipine Besilate IP eq. to Amlodipine 5 mg
Excipients
Colours: Ferric Oxide Yellow USP-NF & Titanium
Dioxide IP
q.s.
Telmisartan and Chlorthalidone Tablets Each uncoated tablet contains
Telmisartan IP 40 mg
Chlorthalidone IP 6.25 mg
Excipients q.s
Telmisartan and Chlorthalidone Tablets Each uncoated tablet contains
Telmisartan IP 40 mg
Chlorthalidone IP 12.5 mg
Excipients q.s
Telmisartan and Cilnidipine Tablets Each film coated tablet contains :
Telmisartan IP 40 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
CARDIAC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Telmisartan, Cilnidipine and Chlorthalidone Tablets Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 5 mg
Chlorthalidone IP 6.25 mg
Telmisartan, Cilnidipine and Chlorthalidone Tablets Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 5 mg
Chlorthalidone IP 12.5 mg
Telmisartan, Cilnidipine and Chlorthalidone Tablets Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 10 mg
Chlorthalidone IP 6.25 mg
Telmisartan, Cilnidipine and Chlorthalidone Tablets Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 10 mg
Chlorthalidone IP 12.5 mg
Telmisartan Tablets IP 40mg Tablets Each uncoated tablet contains:
Telmisartan I.P. 40 mg
Excipients q.s.
DIABETIC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Glimepiride & Metformin HCl (ER) Tablets Each film coated tablet contains:
Glimepiride 1 /2 mg
Metformin Hydrochloride IP
( In Extended release form )
Colour: Titanium Dioxide I.P. & Lake of Indigo - Carmine
500/1000 mg
Pioglitazone HCl & Metformin HCl ER Tablets Each uncoated Bilayered tablets contains:
Pioglitazone HCl
eq. to Pioglitazone 7.5/15 mg
Metformin Hydrochloride IP
( In Extended release form )
Colour: Quinoline Yellow WS
500/1000 mg
Glimepiride Tablets Each uncoated tablet contains:
Glimepiride
Colour: Red Oxide of Iron
1 /2mg
Pioglitazone Hydrochloride Tablets Each uncoated tablet contains:
Pioglitazone Hydrochloride
eq. to Pioglitazone
Colour: Sunset yellow FCF
7-5/15 /30mg
Gliclazide and Metformin Tablets Each uncoated bilayered sustained release tablet contains :
Gliclazide IP (SR) 30 /60 mg
Metformin Hydrochloride IP (SR)
Excipients q.s.
500 mg
Gliclazide Pioglitazone and Metformin Tablets Each uncoated bilayered tablet contains :
Metformin Hydrochloride IP (
in sustained release form )
500 mg
DIABETIC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Gliclazide IP
( in sustained release form )
Pioglitazone Hydrochloride IP equivalent to
60 mg
Pioglitazone Excipients
q.s.
15 mg
Glibenclamide & Metformin HCl (ER) Tablets Each film coated tablet contains:
Glibenclamide 5 mg
Metformin Hydrochloride IP 500 mg
Glimepiride & Metformin HCl (ER) Tablets Each film coated tablet contains:
Glimepiride 1 /2mg
Metformin Hydrochloride IP
( In Extended release form )
Colour: Titanium Dioxide I.P. & Lake of Indigo - Carmine
500/1000 mg
Gliclazide, Metformin HCl and
Pioglitazone HCl Tablets Each uncoated bilayered tablet contains :
Metformin Hydrochloride IP (
in sustained release form )
500 mg
Gliclazide IP
( in sustained release form )
Pioglitazone Hydrochloride IP equivalent to
60 mg
Pioglitazone 7.5 mg
GlimpIride, Metformin HCl , Pioglitazone
HCl and Tablets Each uncoated bilayered tablet contains :
Metformin Hydrochloride IP
( in sustained release form )
Pioglitazone Hydrochloride IP equivalent to
500 mg
Pioglitazone 7.5 mg
DIABETIC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Glimepiride IP
Excipients q.s.
2 mg
Metformin 500 mg Tablets Each uncoated tablet contains:
Metformin hcl 500
Excipients q.s.
Metformin Sustained Release Tablets Each uncoated Sustained released tablet contains:
Metformin Hydrochloride IP 500/1000 mg
GlimepiridePioglitazone & Metformin
HCl SR Tablets Each bilayer tablet contains
Pioglitazone Hydrochloride eq. to Pioglitazone 7.5/15 mg
Glimepiride USP 1/2 mg
Metformin Hydrochloride IP
(In Sustained release form)
Colour: Sunset Yellow FCF.
500/1000 mg
Metformin Hydrochloride and Voglibose Tablets Each uncoated tablet contains:
Voglibose 0.2/0.3 mg
Metformin Hydrochloride IP 500 mg
Excipients
Colour: Tartrazine Yellow
q.s.
Voglibose 0.2 mg Tablets Each uncoated tablet contains
Voglibose 0.2 mg
Excipients q.s.
Voglibose 0.3 mg Tablets Each uncoated tablet contains
DIABETIC PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Voglibose 0.3 mg
Excipients q.s.
Gliclazide ER Tablets 30 mg Tablets Each uncoated tablet contains:
Gliclazide IP (as extended release) 30 mg
Excipients q.s.
Gliclazide ER Tablets 60 mg Tablets Each uncoated tablet contains:
Gliclazide IP (as extended release) 60 mg
Excipients q.s.
Gliclazide ER & Metformin
Hydrochloride ER Tablets Each uncoated bilayered tablet contains:
Gliclazide IP (as extended release) 30 mg
Metformin Hydrochloride IP (as extended release ) 500 mg
Excipients q.s
Gliclazide ER & Metformin
Hydrochloride ER Tablets Each uncoated bilayered tablet contains:
Gliclazide IP (as extended release) 60 mg
Metformin Hydrochloride IP (as extended release ) 500 mg
Excipients q.s
GASTRO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Bisacodyl IP Tablets Each enteric coated tablet contains
Bisacodyl IP
Colours: Tartrazine
5 mg
Clidinium Bromide and Chlordiazepoxide Tablets Each film coated tablet contains:
Clidinium Bromide 2.5 mg
Chlordiazepoxide IP 5 mg
Excipients q.s
Metoclopramide HCl Tablets Each uncoated tablet contains
Metoclopramide Hcl eqv. To anhydrous
metoclopramide HCl 10 mg
Mebeverine hydrochloride + Chlordiazepoxide Tablets Each film coated tablet contains:
Mebeverine hydrochloride IP 135 mg
Chlordiazepoxide IP 5 mg
Excipients q.s
Omeprazole Magnesium & Domperidone Tablets Each enteric coated tablet contains:
Omeprazole Magnesium
eq. to Omeprazole 20 mg.
Domperidone B.P.
Colour : Erythrosine
10 mg.
Pantoprazole Tablets Each gastro resistant (enteric coated) tablet
contains:
Pantoprazole Sodium Sesquihydrate
equivalent to Pantoprazole
Colour: Yellow Oxide Of Iron & Tianium
Dioxide
20 /40 mg.
Pantoprazole & Domperidome Tablets Each gastro resistant (enteric coated) tablet
contains:
Pantoprazole Sodium Sesquihydrate
GASTRO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
equivalent to Pantoprazole 40 mg.
Domperidome
Colour: Yellow Oxide Of Iron & Tianium
Dioxide
10 mg
Ranitidine Hydrochloride and Domperidome Tablets Each Film Coated Tablet Contains:
Ranitidine Hydrochloride I.P.
equivalent to Ranitidine 150 mg
Domperidome
Colour: Lake of Indigo Caramine FCF &
Titanium Dioxide
10 mg
Rabeprazole & Livosulpride (SR) Tablets Each tablet contains
Rabeprazole 40 mg
Livosulpride (SR) 75 mg
Sodium Picosulfate Tablets Each uncoated tablet contains:
Sodium Picosulfate BP 10 mg
Lactulose Solution Solution Each 15 ml. contains:
Lactulose Concentrate U.S.P.
Equivalent to Lactulose 10 gm.
Aqueous base q.s.
Magaldrate, Simethicone & Oxetacaine Suspension Each 5 ml contains: Magaldrate
IP
equivalent to Anhydrous Magaldrate 480 mg
Simethicone IP 20 mg
Oxetacaine BP 10 mg
Flavoured syrupy base
Colour : Quinoline yellow WS
q.s.
Magaldrate, Simethicone and Aluminium HCl Suspension Each 5ml contains
GASTRO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Simethicone IP 250 mg
Magnesium Hydroxide IP
( Added as Magnesium Hydroxide paste )
250 mg
Aluminium Hydroxide Gel IP
( Added as Aluminium Hydroxide paste )
Colour: Erythrosine.
250 mg
Magnesium Hydroxide, Aluminium
Hydroxide, Simethicone & Oxetacaine Gel Gel Each 5ml contains
Magnesium Hydroxide IP 300 mg
Dried Aluminium Hydroxide Gel IP 600 mg
Simethicone IP 25 mg
Oxetacaine BP 10 mg
Milk of Magnesia, Sodium Piosulphate and
Liquid Paraffin Suspension Each 5ml contains:
Liquid Paraffin IP 1.25 ml
Milk of Magnesia IP 3.75 ml
Sodium Picosulphate BP
Colours: Carmoisine & Ponceau 4R.
3.33 mg
Paracetamol Suspension/Syrup Each 5 ml contains:
Paracetamol I.P.
Colour: Ponceau 4R
125 mg
Paracetamol Suspension/Syrup Each 5ml contains:
Paracetamol IP 250 mg
Flavoured Syrup base
Colour: Sunset yellow FCF
q.s.
Simethicone, Dill Oil and Fennel oil Suspension Each ml (approx. 25 drops from enclosed
dropper) contains:
Simethicone Emulsion USP
eq. to Simethicone USP 40 mg
Dill Oil BP 0.005 ml
Fennel Oil IP 66 0.0007 ml
GASTRO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Pantoprazole and Levosulpride Capsules Each Hard gelatin capsule contains Pantoprazole
Sodium IP
equivalent to Pantoprazole 40 mg
Levosulpride
( as enteric coated pallets )
Excipients
Approved colours used in capsule shell
75 mg
Pantoprozole & Domperidone Capsules Each hard gelatin capsule contains: Pantoprazole
Sodium eq. to
Pantoprazole (As enteric coated pellets) 40 mg
Domperidone B.P.
(10mg as immediate release and 10mg as
sustained release pallets)
20 mg
Pantoprazole and Domperidone Capsules Each hard gelatin capsule contains:
Pantoprazole Sodium Sesquihydrate
equivalent to Pantoprazole IP (as Enteric Coated
pellets) 40 mg
Domperidone IP (as sustained release) 30 mg
Rabeprazole Sodium and Itopride HCl Capsules Each capsule contains:
Rabeprazole Sodium (as enteric coated pellets) 20 mg
Itopride Hydrochloride (S.R.)
Approved colours used in capsule shells
150 mg
GYNAE PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Doxylamine Succinate,Pyridoxine HCl and
Folic Acid Tablets Doxylamine Succinate USP 10 mg
Pyridoxine HCl IP 10 mg
Folic Acid IP
Colour: Ferricoxide Red & Titanium Dioxide IP
2.5 mg
Folic Acid,Pyridoxine HCl and Mecobalamin Tablets Each Film Coated Tablet contains:
Folic Acid IP 1.5 mg
Pyridoxine HCl IP 3 mg
Mecobalamin 1500 mcg
Ferrous Ascorbate, Folic Acid & Zinc Tablets Each film coated tablet contains: Ferrous
Ascorbate
eq. to Elemental Iron 100 mg
Folic Acid IP 1.5 mg
Zinc 22-5 mg
Excipients
Colour: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Ferrous Ascorbate, Folic Acid, Mecobalamin
& Zinc
Tablets Each film coated tablet contains:
Ferrous Ascorbate
eq. to Elemental Iron 100 mg
Folic Acid IP 1.5 mg
Mecobalamin 1500 mcg
Zinc 22-5 mg
Excipients
Colour: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Ferrous Ascorbate, Folic Acid, Mecobalamin
& Zinc
Tablets Each film coated tablet contains:
Ferrous Ascorbate
eq. to Elemental Iron 100 mg
GYNAE PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Folic Acid IP 1.1 mg
Mecobalamin 1500 mcg
Zinc 22-5 mg
Excipients q.s.
Ferrous Ascorbate & Folic Acid Tablets Each film coated tablet contains:
Ferrous Ascorbate
eq. to Elemental Iron 100 mg
Folic Acid IP 1.5 mg
Excipients
Colour: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Folic acid Tablets Each film coated tabelt contains
Folic Acid
Colour : Titanium Dioxide IP
5 mg
Sodium Feredetate ,Folic Acid ,Vitamin B12 Tablets Each film coated tablets contains:
Sodium Feredetate BP
( eq. to 33mg Elemental Iron )
231 mg
Folic Acid I.P. 1.5 mg
Vitamin B12 I.P.
Colour: Ponceau 4R
15 mcg
Ferrous Ascorbate Syrup Each 5ml contains:
Ferrous Ascorbate
eq. to Elemental Iron 30 mg
Folic Acid IP 500 mcg
Ferrous Ascorbate & Folic Acid Drops Each ml contains:
Ferrous Ascorbate
eq. to Elemental Iron 10 mg
Ferric Ammonium Citrate and vitamin Syrup Each 5 ml contains:
Ferric Ammonium Citrate I.P. 80 mg
Folic Acid I.P. 0.166 mg
GYNAE PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Vitamin B12 I.P. 1 mcg
Flavoured Syrupy base Colour:
Caramel
q.s.
Ferric Ammonium Citrate and vitamin Syrup Each 5ml (one teaspoonful) contains:
Ferric Ammonium Citrate IP 110 mg
Folic Acid IP 1.5 mg
Cynacobalamin IP 15 mcg
Sorbitol (70%) (Non Crystalline) IP Colour:
Caramal IP
q.s.
Ferrous Bisglycinate Zinc &Vitamin Syrup Each 5ml contains:
Vitamin B 12 IP 15 mcg.
Folic Acid IP
Ferrous Bisglycinate
1500 mcg.
equivalent to elemental Iron Zinc
Bisglycinate
100 mg.
equivalent to elemental Zinc Colour:Ponceau
4-R
15 mg.
Iron, Folic Acid, Vit.B12 & Zinc Pediatric Syrup Each 5ml contains:
Ferrous Bisglycinate
equivalent to elemental Iron 60 mg.
Folic Acid IP 500 mcg.
Vitamin B12 IP Zinc
Bisglycinate
5 mcg.
equivalent to elemental Zinc Colour:Ponceau
4-R
15 mg.
Mecobalamin and Folic acid Syrup Each 5 ml. contains:
Mecobalamin 250 mcg
Folic Acid 1500 mcg
L-Arginine+L-Carnitine+Lycopene+Zinc Sachets Each sachet of 10gms contains
L- Arginine 3 g
GYNAE PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Lycopene (As 10% Powder) 7.5 mg
L-carnitine 500 mg
Zinc 10 mg
Co-enzyme Q10 25 mg
Excipients q.s.
L-Arginine+DHA+Magnesium+Zinc+Folic
Acid Sachets Each sachet of 10gms contains
L- Arginine 3 g
DHA 200 mg
Magnesium 100 mg
Zinc 15 mg
Folic Acid 1.5 mg
Excipients q.s.
L-Arginine Granules Sachet Each Sachet of 5 g contains:
L-Arginine IP 3 g
Excipients q.s
LAXATIVES PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Sodium Picosulphate Oral Solution BP Oral Solution Each 5ml contains:
Sodium Picosulphate BP 5 mg
Exciepients q.s.
LIPID LOWERING PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Atorvastatin Tablets Each Film coated Tablet Contains:
Atorvastatin Calcium Equivalent to Atorvastatin 10 /20/40/80 mg
Excipients
Colour : Titanium Dioxide
q.s.
Atorvastatin & Fenofibrate Tablets Each film coated tablet contains:
Atorvastatin Calcium equivalent to
Atorvastatin 10 mg
Fenofibrate BP (micronised)
Colour: Red oxide of Iron and Titanium Dioxide I.P.
160 mg
Atorvastatin Calcium and Fenofibrate Tablets Each film coated tablet contains:
Atorvastatin Calcium IP equivalent to Atorvastatin 10 mg
Fenofibrate IP (Nano Particle)
Colour: Titanium Dioxide I.P.
145 mg
Atorvastatin & Metformin HCl Tablets Each uncoated bilayered tablet contains:
Atorvastatin Calcium IP eq. to Atorvastatin 10 mg
Metformin Hydrochloride IP(In sustained release form)
Colours: Yellow Oxide of Iron & Titanium Dioxide IP
500/1000 mg
Atorvastatin Calcium and Fenofibrate Tablets Each film coated tablet contains:
Atorvastatin Calcium IP equivalent to Atorvastatin 10 mg
Fenofibrate IP (Nano Particle)
Colour: Titanium Dioxide I.P.
145 mg
Atorvastatin Calcium and Ezetimibe Tablets Each film coated tablet contains:
Atorvastatin Calcium equ. To Atorvastatin 10 /20 mg
Ezetimibe
Colour : Sunset yellow FCF
10 mg
Fenofibrate Tablets Each film coated tablet contains:
Fenofibrate IP (Nano Particle) 145 mg
LIPID LOWERING PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Colour: Titanium Dioxide I.P.
Fenofibrate Tablets Each film coated tablet contains:
Fenofibrate IP (micronised )
Colour: Titanium Dioxide I.P.
160 mg
Rosuvastatin 5/10/20/40 mg IP Tablets Each film coated tablet contains:
Rosuvastatin Calcium IP eq. to Rosuvastatin
Colours: Brilliant Blue & Titanium Dioxide IP
5 /10/20/40 mg
Rosuvastatin & Fenofibrate Tablets Each film coated tablet contains:
Rosuvastatin Calcium IP eq. to Rosuvastatin 5 /10 mg
Fenofibrate BP (Nano Particle)
Colour: Approved colour used
145 mg
Rosuvastatin & Fenofibrate Tablets Each film coated tablet contains:
Rosuvastatin Calcium IP eq. to Rosuvastatin 5 /10 mg
Fenofibrate IP ( Micronised )
Colour: Titanium Dioxide IP
160 mg
Rosuvastatin & Fenofibrate Tablets Each film coated tablet contains:
Rosuvastatin Calcium IP eq. to Rosuvastatin 10 mg
Fenofibrate IP (Nano Particle) 67 mg
Excipients q.s.
Rosuvastatin and Vitamin D3 Tablets Each film coated tablet contains :
Rosuvastatin Calcium I.P
equivalent to Rosuvastatin 5 mg
Vitamin D3 I.P( Cholecalciferol) 1000 IU
Excipients
Approved Colours used
q.s
Rosuvastatin and Vitamin D3 Tablets Each film coated tablet contains :
Rosuvastatin Calcium I.P
equivalent to Rosuvastatin 10 mg
LIPID LOWERING PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Vitamin D3 I.P( Cholecalciferol) 1000 IU
Excipients
Approved Colours used
q.s
Simvastatin Tablets Each film coated tablet contains:
Simvastatin Calcium
Colours: Approved colours used
10/20/40 mg
MALE INFERTILITY PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Dapoxetine Tablets Each film coated tablet contains:
Dapoxetine Hydrochloride Eq. to Dapoxetine 30 /60 mg
Excipients
Colourants: Lake Brilliant Blue & Titanium Dioxide IP
q.s.
Dapoxetine & Sildenafil Citrate Tablets Each tablet contains
Dapoxetine 30 mg
Sildenafil Citrate 50 mg
Dapoxetine & Sildenafil Citrate Tablets Each tablet contains
Dapoxetine 30 mg
Sildenafil Citrate 100 mg
Dapoxetine & Sildenafil Citrate Tablets Each tablet contains
Dapoxetine 60 mg
Sildenafil Citrate 25 /50/100mg
Sildenafil Citrate Tablets Each film coated tablets contains:
Sildenafil Citrate
eqv. To Sildenafil
Colour: Indigo Carmine
10 /25/50/100 mg
MULTI-VITAMIN PRODUCT
RANGE TYPE LABEL CLAIMS STRENGTH
Mecobalamin Tablets Each Film coated tablets contains
Mecobalamin 500/750/1500 mcg
Mecobalamin & Folic Acid Tablets Each Film Coated Tablet contains:
Folic Acid IP 1.5 mg
Mecobalamin
Colour: Titanium Dioxide I.P. & Red Oxide of
Iron
750 mcg
Pyridoxine Tablets Each uncoated tablet contains
Pyridoxine Hcl 25/40/50 mg
Thiamine Hydrochloride Tablets I.P Tablets Each flim coated tablet contains :
Thiamine Hydrochloride I.P 100 mg
Excipients
Approved colours used
q.s
Zinc Tablets Each film coated tablet contains
Zinc (as zinc sulphate) 10 mg
MUSCLE RELAXING PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Tamsulosin HCl Modified Release &
Dutasteride Capsules Each hard gelatin capsule contains:
Tamsulosin Hydrochloride IP (as modified
release tablets) 0.4 mg
Dutasteride
Approved colours used in capsule shell
0.5 mg
Tamsulosin Hydrochloride & Finasteride Capsules Each film coated tablets contains:
Tamsulosin Hydrochloride (
as sustained release )
0.4 mg
Finasteride USP
Colour: Red Oxide of Iron & Titanium Dioxide
I.P.
5 mg
Inositol Nicotinate Tablets BP Tablets Each film coated tablet contains:
Inositol Nicotinate BP 1000 mg
Excipients
Approved colours used
q.s.
NASAL DROPS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Oxymetazoline Hydrochloride Nasal
solution USP Solution Each ml contains:
Oxymetazoline Hydrochloride USP 0.5 mg
NEPHRO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Allopurinol Tablets Each uncoated tablet contains
Allopurinol IP 100 mg
Flavoxate HCl Tablets Each film coated tablet contains:
Flavoxate HCl
Colour: Titanium Dioxide IP
200 mg
Tamsulosin HCl Modified Release Tablets Each film coated modified release tablet contains:
Tamsulosin Hydrochloride
Colours: Quinoline Yellow and Titanium Dioxide IP
0.2/0.4 mg
Tolterodine Tartrate Extended Release Tablets Each uncoated Extended release tablet contains
Tolterodine Tartrate 2 /4 mg
Excipients q.s.
Trospium Chloride Extended Release Tablets Each film coated extended release tablet contains:
Trospium Chloride BP 60 mg
Excipients
Colours: Ponceau 4R & Titanium Dioxide IP
q.s.
Potassium Citrate and Citric Acid Oral
Solution USP
Oral Solution Composition: -
Each 5ml contains:
Potassium Citrate Monohydrate IP 1100 mg
Citric Acid Monohydrate IP 334 mg
Flavoured Sorbitol base
( each ml contains 2ml eq. of Potassium ion )
Colour: Tartrazine
q.s.
Potassium Citrate and Magnesium citrate Syrup Each 5ml contains
Potassium Citrate 1100 mg
Magnesium Citrate 375 mg
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Citicoline Sodium Tablets Each film coated tablet contains:
Citicoline Sodium 500 mg
Excipients
Colour: Yellow Oxide of Iron & Titanium Dioxide IP
q.s.
Citicoline Sodium Sustained Release Tablets Each Sustained release tablet contains
Citicoline Sodium 1000 mg
Citicholine and Piracetam Tablets Tablets Each film coated tablet contains:
Citicholine Sodium eq. to Citicholine 500 mg
Piracetam IP Colour: Brilliant Blue FCF & Titanium Dioxide IP
800 mg
Desvenlafaxine Succinate Tablets Each film coated extended release tablet contains:
Desvenlafaxine Succinate Monohydrate
eq. to Desvenlafaxine 50 /100 mg
Excipients
Colour: Red Oxide of Iron & Titanium Dioxide IP
q.s.
Eslicarbazepine Acetate Tablets Each tablet contains
Eslicarbazepine Acetate 200/400/800 mg
Etizolam Tablets 0.25mg Tablets Each uncoated tablet Contains
Etizolam JP 0.25 mg
Excipients q.s.
Etizolam Tablets 0.5mg Tablets Each uncoated tablet Contains
Etizolam JP 0.5 mg
Excipients q.s.
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Etizolam Tablets 1mg Tablets Each uncoated tablet Contains
Etizolam JP 1 mg
Excipients q.s.
Flupenthixol and Melitracen Tablets Each film coated tablets contains: Flupenthixol
Dihydrochloride
eq. to Flupenthixol Melitracen
Hydrochloride
0.5 mg
eq. to Melitracen Colour: Erythrosine and Indigocarmine
10 mg
Levetiracetam Tablets Each flim coated tablet contains :
Levetiracetam USP 250 mg
Excipients Approved colours used
q.s
Levetiracetam Tablets Each flim coated tablet contains :
Levetiracetam USP 1000 mg
Excipients Approved colours used
q.s
Lamotrigine Dispersible tablets IP 100 mg
Tablets Each uncoated Dispersible Tablet Contains
Lamotrigine IP 100 mg
Excipients q.s.
Lamotrigine tablets 50mg Tablets Each dispersible tablets contains
Lamotrigine 50 mg
Excipients q.s.
NEURO PRODUCT RANGE TYPE LABEL CLAIMS
STRENGTH
Lamotrigine Dispersible tablets IP 25mg Tablets Each uncoated Dispersible Tablet Contains
Lamotrigine IP 25 mg
Excipients q.s.
Lamotrigine Sustained Release tablets IP
100 mg Tablets Each uncoated Sustained Release Tablet Contains
Lamotrigine IP 100 mg
Excipients q.s.
Lamotrigine Sustained Release tablets IP
150 mg Tablets Each uncoated Sustained Release Tablet Contains
Lamotrigine IP 150 mg
Excipients q.s.
Lamotrigine Sustained Release tablets IP
200 mg Tablets Each uncoated Sustained Release Tablet Contains
Lamotrigine IP 200 mg
Excipients q.s.
Lamotrigine Sustained Release tablets IP 50 mg
Tablets Each uncoated Sustained Release Tablet Contains
Lamotrigine IP 50 mg
Excipients q.s.
Methyldopa Tablets Each film coated tablet contains:
Metyldopa eq. to anhydrous methydopa Colour:
Titanium Dioxide I.P.
250
Oxcarbazepine Tablets Each film coated tablet contains:
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Oxcarbazepine IP
Colour: Yellow oxide of Iron & Titanium Dioxide IP
150/300/600 mg
Olanzapine Tablets IP 2.5mg Tablets Each uncoated tablet contains
Olanzapine IP 2.5 mg
Excipients q.s.
Olanzapine Tablets IP 5mg Tablets Each uncoated tablet contains
Olanzapine IP 5 mg
Excipients q.s.
Olanzapine Tablets IP 7.5mg Tablets Each uncoated tablet contains
Olanzapine IP 7.5 mg
Excipients q.s.
Olanzapine Tablets IP 10mg Tablets Each uncoated tablet contains
Olanzapine IP 10 mg
Excipients q.s.
Olanzapine Tablets IP 15mg Tablets Each uncoated tablet contains
Olanzapine IP 15 mg
Excipients q.s.
Olanzapine Tablets IP 20mg Tablets Each uncoated tablet contains
Olanzapine IP 20 mg
Excipients q.s.
Opipramol Dihydrochloride Tablets Each Film coated tablet contains
Opipramol Dihydrochloride 50 mg
Excipients q.s
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Approved Colours used
Opipramol Dihydrochloride Tablets Each Film coated tablet contains
Opipramol Dihydrochloride 100 mg
Excipients
Approved Colours used
q.s
Oxcarbazepine Sustained Realese tablet
150mg Tablets Each film coated sustained release tablet contains:
Oxcarbazepine IP 150 mg
Excipients q.s.
Oxcarbazepine Sustained Realese tablet
300mg Tablets Each film coated sustained release tablet contains:
Oxcarbazepine IP 300 mg
Excipients q.s.
Oxcarbazepine Sustained Realese tablet
450mg Tablets Each film coated sustained release tablet contains:
Oxcarbazepine IP 450 mg
Excipients q.s.
Oxcarbazepine Sustained Realese tablet
600mg Tablets Each film coated sustained release tablet contains:
Oxcarbazepine IP 600 mg
Excipients q.s.
Sevelamer Carbonate Tablets Each film coated tablet contains:
Sevelamer Carbonate 400/800 mg
Excipients q.s.
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Colours: Ferric Oxide Yellow NF USP & Titanium Dioxide
IP
Zolpidem Tartrate Tablets IP Tablets Each film coated tablet contains
Zolpidem Tartrate IP
Colours: Approved Colours used
5 /10mg
Gabapentin Capsules Each Capsule contains:
Gabapentin
Approved colours used in capsule shells
300 mg
Pregabalin Capsules Each Capsule contains:
Pregabalin
Approved colours used in capsule shells Pregabalin
Capsules
75 mg
Pregabalin Capsules Each Capsule contains:
Pregabalin Approved colours used in capsule shells
150 mg
Pregabalin & Mecobalamin Capsules Each hard gelatin capsule contains:
Pregabalin 75 mg
Mecobalamin 750 mcg
Excipients
Approved colours used in capsule shells
q.s.
Pregabalin & Mecobalamin Capsules Each hard gelatin capsule contains:
Pregabalin 150 mg
Mecobalamin 750 mcg
Excipients
Approved colours used in capsule shells
q.s.
NEURO PRODUCT RANGE TYPE LABEL CLAIMS
STRENGTH
Myo-Inositol Tablets Each tablet contains
Myo-Inositol 1 gm
Myo-Inositol Tablets Each tablet contains
Myo-Inositol 1 gm
Folic Acid 1.5 mg
Gabapentin and Amitriptyline Tablets Each uncoated bilayer tablet contains :
Gabapentin USP 300 mg
Amitriptyline Hydrochloride IP 10 mg
Excipients
Approved Colours used
q.s
Gabapentin and Nortriptyline Tablets Each film coated tablet contains :
Gabapentin USP 400 mg
Nortriptyline Hydrochloride IP eq. to Nortriptyline
10 mg
Excipients
Approved Colours used
q.s
Nortriptyline and Pregabalin Tablets Each film coated tablet contains :
Nortriptyline Hydrochloride IP eq. to Nortriptyline
10 mg
Pregabalin IP 75 mg
Excipients Approved Colours used
q.s
Aceclofenac SR and Pregabalin SR Tablets Each bilayered sustained release tablet contains :
Aceclofenac I.P 200 mg
Pregabalin I.P 75 mg
NEURO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Excipients Approved colours used
q.s
Oxaceprol Capsules Each hard gelatin Capsule contains
Oxaceprol . 200 mg
Excipients
Approved Colours used in Capsule shell
q.s
Citicoline Sodium and Mecobalamin Tablets Each film coated tablet contains: Citicoline
Sodium IP
Equivalent to Citicoline 500 mg
Mecobalamin JP 750 mcg
Excipients
Approved colours used
q.s.
NUTRACEUTICALS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Polyethylene glycol,Sodium Chloride,
Sodium Bicarbonate & Potassium Chloride
Concentrate for Oral Solution
Oral Solution
Each 25 ml of solution contains :
Polyethylene glycol 3350 USP 13.125 gm
Sodium Chloride IP 0.3507 gm
Sodium Bicarbonate IP 0.1785 gm
Potassium Chloride IP 0.0466 gm
Carbonyl Iron, Folic Acid, Calcium, Biotin,
Mecobalamin & Vitamins Capsules Each hard gelatin capsule contains:
Carbonyl Iron 60 mg
Folic Acid IP 10 mg
Calcium Pantothenate 6 mg
Biotin 600 mcg
Mecobalamin 500 mcg
Vitamin B1 2 mg
Vitamin B2 3 mg
Vitamin B3 25 mg
Vitamin B6 10 mg
Execipients
Approved colours used in capsule shell
q.s
Calcium Citrate,Methylcobalam, Calcitriol,
Zinc and Magnesium Hydroxide
Tablets Each film coated tablet contains :
Calcium Citrate USP 1250 mg
Methylcobalamin JP 1500 mcg
Calcitriol IP
Zinc sulphate monohydrate IP
0.25 mcg
equivalent to Elemental Zinc 4 mg
Magnesium Hydroxide IP 100 mg
Excipients
Approved Colours used
q.s
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Calcium Citrate , Vitamin D3,Magnesium
Hydroxide & Zinc Sulphate Tablets Each uncoated tablet contains:
Calcium Citrate U.S.P. 1000 mg
Vitamin D3 I.P.
Magnesium Hydroxide I.P.
200 IU
equivalent to Elemental Magnesium 100 mg
Zinc Sulphate I.P. equivalent to Elemental Zinc 4 mg.
Calcium Carbonate and Alfacalcidol Tablets Each film-coated tablet contains:
1.25 g of Calcium Carbonate from an organic
source (Oystershell)
eq. to Elemental Calcium 500 mg
Alfacalcidol BP 0.25 mcg
Excipients
Colour: Erythrosine & Titanium Dioxide I.P.
q.s.
Alfacalcidol and Calcium Carbonate Tablets Each film coated tablet contains:
Alfacalcidol B.P. 0.25 mcg.
Calcium Carbonate I.P. 625 mg.
equivalent to elemental calcium
Colour: Yellow oxide of iron & Titanium Dioxide
250 mg.
Calcitriol and Calcium Carbonate Tablets Each Film Coated tablet Contains
Calcitriol B.P. 0.25 mcg
Calcium Carbonate I.P.
Colour: Titanium Dioxide
1000 mg
Calcium Carbonate and Vitamin D3 Tablets Each film coated tablet contains:
Calcium Carbonate I.P. (1250mg)
equivalent to elemental calcium 500 mg
Vitamin D3 (Stabilised) IP
Colour: Yellow oxide of iron & Titanium Dioxide I.P.
250 I.U.
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Calcium Citrate,Methylcobalam,
Calcitriol, Zinc and Magnesium Hydroxide
Tablets Each film coated tablet contains :
Calcium Citrate USP 1250 mg
Methylcobalamin JP 1500 mcg
Calcitriol IP
Zinc sulphate monohydrate IP
0.25 mcg
equivalent to Elemental Zinc 4 mg
Magnesium Hydroxide IP 100 mg
Excipients
Approved Colours used
q.s
Calcium, Magnesium, Zinc & Vitamin D3 Tablets Each film coated tablet contains
Calcium Carbonate IP (Precipitated )
eq. to Elemental Calcium 500 mg
Magnesium Hydroxide IP eq. to elemental Magnesium 50 mg
Zinc Sulphate Monohydrate IP eq. to Elemental Zinc 10 mg
Vitamin D3 IP (as Stabilized) 1000 IU
Cholecalciferol Tablets Each uncoated chewable tablet contains:
Cholecalciferol IP (as stabilized) Colour: Sunset
Yellow FCF
1000 IU
Cholecalciferol Tablets Each uncoated chewable tablet contains:
Cholecalciferol IP (as stabilized) Colour: Sunset
Yellow FCF
2000 IU
Cholecalciferol Tablets Each uncoated chewable tablet contains:
Cholecalciferol IP (as stabilized) Colour: Sunset
Yellow FCF
60 ,000 IU
Diacerin & Glucosamine Sulphate
Potassium Chloride Tablets Each film coated tablet contains
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Diacerein 50 mg
Glucosamine Sulphate Potassium Chloride USP 500/750/1500 mg
Diacerin, Glucosamine Sulphate KCl &
MSM Tablets Each tablet contains
Diacerein 50 mg
Glucosamine Sulphate Potassium Chloride USP 500/750/1500 mg
Methyl suphonyl methane 250 mg
Gabapentin Tablets Each film coated tablet contains:
Gabapentin 300/400 mg
Excipients
Colour: Ponceau 4R & Titanium Dioxide IP
q.s.
Gabapentin and Amitriptyline Tablets Each uncoated bilayer tablet contains :
Gabapentin USP 300 mg
Amitriptyline Hydrochloride IP 10 mg
Excipients
Approved Colours used
q.s
Gabapentin and Nortriptyline Tablets Each film coated tablet contains :
Gabapentin USP 400 mg
Nortriptyline Hydrochloride IP eq. to Nortriptyline 10 mg
Excipients
Approved Colours used
q.s
Gabapentin Tablets USP Tablets Each film coated tablet contains:
Gabapentin USP 100 mg
Excipients q.s.
Gabapentin Tablets USP Tablets Each film coated tablet contains:
Gabapentin USP 200 mg
Excipients q.s
Gabapentin Tablets USP Tablets Each film coated tablet contains:
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Gabapentin USP 300 mg
Excipients q.s
Nortriptyline and Pregabalin Tablets Each film coated tablet contains :
Nortriptyline Hydrochloride IP eq. to Nortriptyline 10 mg
Pregabalin IP 75 mg
Excipients
Approved Colours used
q.s
Calcium with Vit. D3 Suspension Each 5ml contains:
Calcium Carbonate I.P.
equivalent to elemental calcium 250 mg
Vitamin D3 IP 125 I.U.
Flavoured Syrupy base q.s.
Calcium Citrate with Vitamin D3 Suspension Each 5ml contains:
Calcium Citrate U.S.P.
eq. to elemental Calcium 100 mg
Vitamin D3 I.P. 200 IU
Flavoured syrupy base q.s.
Liquid Calcium with Phosphorus,
Magnesium, Zinc & Vitamin D3 Suspension Each 10ml contains
Calcium Phosphate IP eq. to Elemental Calcium 300 mg
eq. to elemental Phosphorus 150 mg
Magnesium Hydroxide IP eq. to elemental Magnesium 75 mg
Zinc Gluconate USP eq. to elemental Zinc 4 mg
Vitamin D3 IP 200 IU
Cholecalciferol Oral Solution Each ml contains
Cholecalciferol IP (as stabilized) 400 IU
In a flavoured Syrupy base
Colour : Tartrazine
q.s.
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Cholecalciferol Syrup Each 5ml contains
Cholecalciferol IP (as stabilized) 400 IU
In a flavoured Syrupy base
Colour : Tartrazine
q.s.
Calcium with vitamanin and minerals Suspension For therapeutic use
Each 5ml (1 teaspoonful) contains:
Calcium Carbonate I.P.
equivalent to elemental calcium
Magnesium Hydroxide I.P.
150 mg
equivalent to Elemental Magnesium
Zinc Gluconate USP
25 mg
eq. to elemental Zinc 1.5 mg
Vitamin D3 IP 200 I.U
Flavoured Syrupy base q.s.
Vitamin D3 Oral Solution Each 5 ml contains :
Cholecalciferol IP
( in Nano Droplet form )
60000 IU
in a Flavoured Syrupy base
Approved Colours used
q.s
Diacerein 50 mg Capsules Each hard gelatin capsule contains:
Diacerein
Approved colours used in capsule shells
50 mg
Cholecalciferol Sachets Each Sachet of 1gm contains:
Cholecalciferol IP (Stabilized) 60 ,000 IU
Excipients
Appropriate overages added
q.s.
Collagen+Glucosamine+Vit C Sachets Each sachet of 12gms contains
Glucosamine Sulphate Potassium Chloride 1500 mg
Collagen Peptide 10 g
Vitamin C 35 mg
ORTHO PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Collagen Peptide Sachets Each sachet of 12gms contains
Collagen Peptide
Appropriate overages added
10 g
Cholecalciferol Mouth Dissolving Tablets
60,000 IU
Tablet
Each uncoated mouth dissolving tablet contains:
Cholecalciferoi 1.P. (as stabilized)
60000 I.U
Excipients
Approved colours used
q.s.
Calcium and Vitamin 03 Tablets Each film coated tablet contains:
Elemental Calcium from
Coral Grains
500 mg
Cholecalciferol 1.P. (as stabilized) 1000 mg
Excipients
Approved colours used
q.s.
PAEDIATRIC PRODUCT RANGE TYPE LABEL CLAIMS
STRENGTH
Zinc Gluconate USP Syrup Each 5ml (1 teaspoonful) contains:
Zinc Gluconate USP
eq. to elemental Zinc 4 mg
Flavoured Syrupy base q.s.
Zinc Gluconate Syrup Each 5 ml contains:
Zinc Gluconate U.S.P. equivalent
to elemental Zinc in a flavoured syrupy base
Approved colours used
20 mg
WEIGHT LOSS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Febuxostat Tablets 80 mg/120 mg Tablets Each film coated tablet contains:
Febuxostat
Colour: Approved colour used
40 /80/120 mg
HEMATINICS PRODUCT RANGE TYPE LABEL CLAIMS STRENGTH
Sodium Ferriditate & Folic Acid & Vit Syrup Each 5ml contains:
Sodium Feredetate BP
( eq. to 33mg Elemental Iron )
231 mg
Folic Acid I.P. 1.5 mg
Vitamin B12 I.P. 15 mcg
Excipients q.s.
Sodium Feredetate Oral Solution B.P. Oral Solution Each 15ml (1 tablespoonful) contains
Sodium Feredetate B.P.
( Eq. to 33mg of elemental Iron )
231 mg
Flavoured Syrupy base q.s.
Iron with Folic Acid and Zinc Capsules Each Capsule contains:
Elemental Iron (in the form of carbonyl Iron) 100 mg
Folic Acid IP 1 mg
Vitamin B12 IP 5 mcg
Selenium (as Sodium Selenite Pentahydrate BP) 65 mcg
Zinc Sulphate Monohydrate USP
( eq. to 15.6mg of elemental Zinc )
Approved colours used in capsule shells
43 mg
Iron & Vitamin Capsules Each Capsule Contains
Carbonyl Iron
( equivalent to 60 mg of Elemental Iron )
62 mg
Folic Acid I.P. 1000 mcg
Vitamin B 12 I.P. 5 mcg
Selenium
( as Sodium Selenite Pentahydrate B.P )
Approved colours used in capsule shells
60 mcg
LIVER RELATED PRODUCT
RANGE
TYPE LABEL CLAIMS STRENGTH
Silymarin Tablets Each film coated tablet contains:
Silmarin (as silybin) Colour: Titanium Dioxide I.P.
70/140 mg
Ursodeoxycholic Acid SR Tablets Each Sustained release film coated tablet contains:
Ursodeoxycholic Acid Colour:Titanium Dioxide IP
450/500/600 mg
Ursodeoxycholic Acid and Silymarin Tablets
Each film coated tablet contains :
Ursodeoxycholic Acid IP 300 mg
Silymarin 140 mg
Excipients Approved Colours used
q.s
Silymarin Each 5 ml contains Silmarin Colour: Titanium Dioxide I.P.
Liver Tonic Tonic Each 5 ml contains
Liver Fraction 2* ( Derived from 0.1g of fresh liver )
4.0 mg
Yeast Extract* 46.39 mg
Alcohol IP 10 %v/v
Flavoured Syrupy base Approved Colours used ( * Estimated as total Nitrogen content )
q.s
Ursodeoxychollc Acid Tablets IP Tablets Each film coated tablet contains
Ursodeoxycholic Acid IP Excipients Approved colours used
150 mg q.s.
Ursodeoxychollc Acid Tablets IP Tablets Each film coated tablet contains
Ursodeoxycholic Acid IP 300 mg
Excipients Approved colours used
q.s.
S.No Name of Product Strength
1 Levetiracetam Tablets Each flim coated tablet contains :
Levetiracetam USP 250 mg
Excipients Approved colours used
q.s
2 Levetiracetam Tablets Each flim coated tablet contains :
Levetiracetam USP 1000 mg
Excipients Approved colours used
q.s
3 Montelukast, Levocetirizine and Acebrophylline (SR) Tablets
Each film coated bilayered tablet contains : Montelukast Sodium
IP
equivalent to Montelukast 10 mg
Levocetirizine Hydrochloride IP
Acebrophylline
5 mg
( sustained release form) 200 mg
Excipients
Approved Colours used
q.s
4 Prochlorperazine Maleate Mouth Dissolving Tablets
Each uncoated tablet contains :
Prochlorperazine maleate IP 5 mg
Excipients q.s.
5 Ursodeoxycholic Acid and Silymarin Tablets
Each film coated tablet contains :
Ursodeoxycholic Acid IP 300 mg
Silymarin 140 mg
Excipients Approved Colours used
q.s
6 Gabapentin and Amitriptyline Tablets
Each uncoated bilayer tablet contains :
Gabapentin USP 300 mg
Amitriptyline Hydrochloride IP 10 mg
Excipients
Approved Colours used
q.s
7 Thiocolchicoside, Aceclofenac and Paracetamol Tablets
Each film coated tablet contains :
Thiocolchicoside IP 4 mg
Aceclofenac IP 100 mg
Paracetamol IP 325 mg
Excipients
Approved Colours used
q.s
8 Thiocolchicoside, Aceclofenac and Paracetamol Tablets
S.No Name of Product Strength
Each film coated tablet contains :
Thiocolchicoside IP 8 mg
Aceclofenac IP 100 mg
Paracetamol IP 325 mg
Excipients
Approved Colours used
q.s
9 Gabapentin and Nortriptyline Tablets
Each film coated tablet contains :
Gabapentin USP 400 mg
Nortriptyline Hydrochloride IP eq. to Nortriptyline 10 mg
Excipients Approved Colours used
q.s
10 Nortriptyline and Pregabalin Tablets
Each film coated tablet contains :
Nortriptyline Hydrochloride IP eq. to Nortriptyline 10 mg
Pregabalin IP 75 mg
Excipients Approved Colours used
q.s
11 Aceclofenac SR and Pregabalin SR Tablets Each bilayered sustained release tablet contains :
Aceclofenac I.P 200 mg
Pregabalin I.P 150 mg
Excipients Approved colours used
q.s
12 Aceclofenac SR and Pregabalin SR Tablets Each bilayered sustained release tablet contains :
Aceclofenac I.P 200 mg
Pregabalin I.P 75 mg
Excipients Approved colours used
q.s
15 Trypsin, Bromelain, Rutoside Trihydrate & Diclofenac Sodium Tablets
Each enteric coated tablet contains :
Trypsin B.P 48 mg
Bromelain 90 mg
Rutoside Trihydrate B.P 100 mg
Diclofenac Sodium I.P 50 mg
Excipients
Approved colours used
q.s
16 Trypsin -Chymotrypsin with Paracetamol and Aceclofenac Tablets
Each film coated tablet contains :
Aceclofenac I.P 100 mg
Paracetamol I.P 50.000 units Armour units enzymatic activity
(Supplied by a purified concentrate which has specific Trypsin
& Chymotrypsin activity in a ratio of approximately six to one )
325 mg
S.No Name of Product Strength
( As enteric coated granules )
Excipients Approved colours used
q.s
17 Rosuvastatin and Vitamin D3 Tablets
Each film coated tablet contains :
Rosuvastatin Calcium I.P
equivalent to Rosuvastatin 5 mg
Vitamin D3 I.P( Cholecalciferol) 1000 IU
Excipients
Approved Colours used
q.s
18 Rosuvastatin and Vitamin D3 Tablets
Each film coated tablet contains :
Rosuvastatin Calcium I.P
equivalent to Rosuvastatin 10 mg
Vitamin D3 I.P( Cholecalciferol) 1000 IU
Excipients
Approved Colours used
q.s
19 Thiamine Hydrochloride Tablets I.P
Each flim coated tablet contains :
Thiamine Hydrochloride I.P 100 mg
Excipients Approved colours used
q.s
20
Calcium Citrate,Methylcobalam, Calcitriol, Zinc and Magnesium
Hydroxide Tablets
Each film coated tablet contains :
Calcium Citrate USP 1250 mg
Methylcobalamin JP 1500 mcg
Calcitriol IP Zinc sulphate monohydrate IP
0.25 mcg
equivalent to Elemental Zinc 4 mg
Magnesium Hydroxide IP 100 mg
Excipients
Approved Colours used
q.s
21 Vitamin D3 Oral Solution
Each 5 ml contains :
Cholecalciferol IP
( in Nano Droplet form )
60000 IU
in a Flavoured Syrupy base Approved
Colours used
q.s
S.No Name of Products Strength
S.No Name of Product Strength
23 Telmisartan and Cilnidipine Tablets
Each film coated tablet contains :
Telmisartan IP 40 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
24 Telmisartan and Chlorthalidone Tablets
Each uncoated tablet contains
Telmisartan IP 40 mg
Chlorthalidone IP 6.25 mg
Excipients q.s
25 Telmisartan and Chlorthalidone Tablets
Each uncoated tablet contains
Telmisartan IP 40 mg
Chlorthalidone IP 12.5 mg
Excipients q.s
26 Olmesartan Medoxomil and Cilnidipine Tablets Each film coated tablet contains
Olmesaratan Medoxomil BP 20 mg
Cilnidipine 10 mg
Excipients Approved Colours used
q.s
27 Olmesartan Medoxomil and Cilnidipine Tablets
Olmesaratan Medoxomil BP 40 mg
Cilnidipine 10 mg
Excipients Approved Colours used
q.s
28 Cilnidipine and Nebivolol Tablets Each film coated Bilayered tablet contains :
Nebivolol Hydrochloride IP
equivalent to Nebivolol 2.5 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
29 Cilnidipine and Nebivolol Tablets Each film coated Bilayered tablet contains :
Nebivolol Hydrochloride IP
equivalent to Nebivolol 5 mg
Cilnidipine 10 mg
Excipients
Approved Colours used
q.s
30 Opipramol Dihydrochloride Tablets
Each Film coated tablet contains
Opipramol Dihydrochloride 50 mg
S.No Name of Product Strength
Excipients
Approved Colours used
q.s
31 Opipramol Dihydrochloride Tablets
Each Film coated tablet contains
Opipramol Dihydrochloride 100 mg
Excipients
Approved Colours used
q.s
32 Oxaceprol Capsules Each hard gelatin Capsule contains
Oxaceprol . 200 mg
Excipients Approved Colours used in Capsule shell
q.s
33 Cilnidipine and Metoprolol Succinate ER Tablets
Each film coated bilayered tablet contains :
Cilnidipine 10 mg
Metoprolol Succinate USP 23.75 mg
equivalent to metoprolol tartrate (
in extended release form )
25 mg
Excipients
Approved Colours used
q.s
34 Cilnidipine and Metoprolol Succinate ER Tablets
Each film coated bilayered tablet contains :
Cilnidipine 10 mg
Metoprolol Succinate USP 47.5 mg
equivalent to metoprolol tartrate (
in extended release form )
50 mg
Excipients
Approved Colours used
q.s
35 Polyethylene glycol,Sodium Chloride, Sodium Bicarbonate & Potassium Chloride Concentrate for Oral Solution
Each 25 ml of solution contains :
Polyethylene glycol 3350 USP 13.125 gm
Sodium Chloride IP 0.3507 gm
Sodium Bicarbonate IP 0.1785 gm
Potassium Chloride IP 0.0466 gm
36 Telmisartan, Cilnidipine and Chlorthalidone Tablets
Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 5 mg
Chlorthalidone IP 6.25 mg
37 Telmisartan, Cilnidipine and Chlorthalidone Tablets
Each film coated tablet contains
Telmisartan IP 40 mg
S.No Name of Product Strength
Cilnidipine 5 mg
Chlorthalidone IP 12.5 mg
38 Telmisartan, Cilnidipine and Chlorthalidone Tablets
Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 10 mg
Chlorthalidone IP 6.25 mg
39 Telmisartan, Cilnidipine and Chlorthalidone Tablets
Each film coated tablet contains
Telmisartan IP 40 mg
Cilnidipine 10 mg
Chlorthalidone IP 12.5 mg
40 Pantoprazole and Levosulpride Capsules Each Hard gelatin capsule contains
Pantoprazole Sodium IP
equivalent to Pantoprazole 40 mg
Levosulpride
( as enteric coated pallets )
Excipients Approved colours used in capsule shell
75 mg
41 Nebivolol and Chlorthalidone Tablets
Each uncoated tablet contains :
Nebivolol Hydrochloride IP
equivalent to Nebivolol 5 mg
Chlorthalidone IP
Excipients
12.5 mg
42 Liver Tonic Each 5 ml contains
Liver Fraction 2* ( Derived from 0.1g of fresh liver )
4.0 mg
Yeast Extract* 46.39 mg
Alcohol IP 10 %v/v
Flavoured Syrupy base Approved Colours used
( * Estimated as total Nitrogen content )
q.s
43 Ursodeoxychollc Acid Tablets IP
Each film coated tablet contains
:
Ursodeoxycholic Acid IP Excipients
Approved colours used
150 mg q.s.
44 Ursodeoxychollc Acid Tablets IP
Each film coated tablet contains
:
Ursodeoxycholic Acid IP 300 mg
S.No Name of Product Strength
Excipients
Approved colours used
q.s.
45 Norfloxacin and Tinidazole Tablets Each
film coated tablet contains:
Norfloxacin IP 400 mg
Tinidazole IP Excipients
Approved colours used
600 mg
46 Zinc Gluconate Syrup Each 5
ml contains:
Zinc Gluconate U.S.P. equivalent to elemental Zinc in a flavoured syrupy base Approved
colours used
20 mg
47 L-Arginine Granules Each Sachet of 5 g contains:
L-Arginine IP 3 g
Excipients q.s
48 Mlnocycline Hydrochloride Tablets USP Each
film coated tablet contains:
Minocycline Hydrochloride USP equivalent to
Minocyclino
100 mg
Excipients
Approved colours used
q.s.
49 Cholecalciferol Mouth Dissolving Tablets 60,000 IU
Each uncoated mouth dissolving tablet contains: Cholecalciferoi
1.P. (as stabilized)
60000 I.U
Excipients
Approved colours used
q.s.
50 Saccharomyces Boulardii 250 MG Each
sachet contains:
Lyophiilised Saccharomyces Boulardii 250 mg
Excipients q.s
51 Calcium and Vitamin 03 Tablets Each
film coated tablet contains:
Elemental Calcium from
Coral Grains
500 mg
Cholecalciferol 1.P. (as stabilized) 1000 mg
S.No Name of Product Strength
Excipients
Approved colours used
q.s.
52 Citicoline Sodium and Mecobalamin tablets
Each film coated tablet contains: Citicoline Sodium
IP
Equivalent to Citicoline 500 mg
Mecobalamin JP 750 mcg
Excipients
Approved colours used
q.s.
53 Inositol Nicotinate Tablets BP Each
film coated tablet contains:
Inositol Nicotinate BP 1000 mg
Excipients
Approved colours used
q.s.
54 Tapentadol Tablets 50 mg Each film coated tablet contains :
Tapentadol Hydrochloride IP equivalent to Tapentadol 50 mg
Excipients Approved colours used
q.s.
55 Tapentadol Tablets 50 mg Each film coated tablet contains :
Tapentadol Hydrochloride IP equivalent to Tapentadol 100 mg
Excipients
Approved colours used
q.s.
56 Ranitidine Oral Solution USP Each
Sml contains:
Ranitidine Hyrochloride IP Equivalent to Ranitidine
Flavoured Syrupy base 75 mg
Approved Colours used q.s
Concern person Zone wise
For North Zone :-
Call Mr. Sharat Singh
Cell no- 07837855001
For South Zone :-
Call Mr. Sumit Sadhotra
Cell no- 08492014608
For West Zone :-
Call Mr. Imran Sheikh
Cell no- 09967861660