Fabriqué en Inde. Reconnu dans plus de 20 pays.
Nous fournissons des formes pharmaceutiques finies directement aux importateurs et distributeurs, ainsi que par l’intermédiaire d’exportateurs négociants, en Afrique, en Asie, au Moyen-Orient, dans la CEI et en Amérique latine.
CEI
- Tadjikistan
- Turkménistan
- Azerbaïdjan Enregistrement
Asie
- Afghanistan
- Myanmar
- Laos
- Cambodge
- Philippines Enregistrement
- Bhoutan Enregistrement
Moyen-Orient
- Irak
- Yémen Enregistrement
- Liban Enregistrement
Afrique
- Angola
- RD Congo
- Zambie
- Madagascar
- Cameroun
- Nigeria
- Somalie
- Rwanda
- Libye
- Tanzanie Enregistrement
Europe
- Portugal
Amérique latine
- Salvador Enregistrement
- Honduras Enregistrement
- Guatemala Enregistrement
Caraïbes
- Jamaïque Enregistrement
Deux voies d’accès au marché, entièrement documentées.
Export direct
Nous approvisionnons directement les importateurs et distributeurs agréés, avec la documentation réglementaire issue de notre propre usine.
Exportateurs négociants
Nous fabriquons pour des exportateurs indiens titulaires d’enregistrements sur leurs marchés, qui disposent ainsi d’une source fiable certifiée BPF-OMS.
Appui à l’enregistrement
Dossiers de lots, certificats d’analyse, certificats BPF et documents techniques pour appuyer l’enregistrement des produits auprès des autorités de santé.
Produits approuvés pour l’export.
100+ dossiers CTD prêts pour l’enregistrement. Certificats d’analyse et prix sur demande.
Les produits sont désignés par leur dénomination internationale (DCI), en anglais.
281 sur 281 produits · 22 classes thérapeutiques
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Each film coated tablet contains:
Aceclofenac BP100 mgParacetamol BP325 mgSerratiopeptidase10 mg(equivalent to 20,000 enzymatic units) (as enteric coated form)
Excipientsq.s.Approved colours used in coating.
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Each hard gelatin capsule contains:
Celecoxib BP/USP200 mgExcipientsq.s.Approved colors used in empty capsule shells.
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Composition:
Diclofenac Diethylamine BP1.16% w/wEq. to Diclofenac Sodium1% w/wIn gel baseq.s. -
Composition:
Diclofenac Diethylamine BP4.64% w/wequivalent to Diclofenac Sodium4.0% w/wMethyl Salicylate BP10.0% w/wMenthol USP5.0% w/wLinseed Oil BP3.0% w/wBenzyl Alcohol USP1.0% w/w(as preservative)
Excipientsq.s.In Gel Base
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Composition:
Diclofenac Diethylamine BP1.16% w/wEq. to Diclofenac Sodium1% w/wLinseed Oil BP3% w/wMethyl Salicylate BP10% w/wMenthol USP5% w/wBenzyl Alcohol BP1% w/w(as preservative)
In gel baseq.s. -
Composition:
Diclofenac Diethylamine BP1.16% w/wEq. to Diclofenac Sodium1% w/wOleum Lini3% w/wMethyl Salicylate BP10% w/wMenthol USP5% w/wBenzyl Alcohol BP1% w/w(as preservative)
In gel baseq.s. -
Composition:
Diclofenac Diethylamine IP4.64% w/wequivalent to Diclofenac Sodium IP4.0% w/wMethyl Salicylate IP10.0% w/wMenthol IP5.0% w/wOleum Lini BP3.0% w/wBenzyl Alcohol IP1.0% w/w(as preservative)
Excipientsq.s.In Gel Base
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Each film coated tablet contains:
Diclofenac Potassium BP/USP50 mgParacetamol BP/USP325 mgChlorzoxazone USP250 mgExcipientsq.s.Approved colors used in coating.
-
Each bilayered uncoated tablet contains:
Diclofenac Sodium BP/USP50 mgParacetamol BP/USP500 mgExcipientsq.s.Approved colours used.
-
Each uncoated tablet contains:
Diclofenac Sodium BP50 mgParacetamol BP500 mgExcipientsq.s. -
Each sustained release film coated tablet contains:
Diclofenac Sodium BP/USP100 mgExcipientsq.s.Approved colors used in coating.
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Composition:
Diclofenac Diethylamine BP1.16% w/weq. to Diclofenac Sodium1.0% w/wMethyl Salicylate BP8.0% w/wMenthol USP2.0% w/wGel baseq.s. - Each film coated tablet contains: Etoricoxib120 mgExcipientsq.s.
Approved colour used in coating.
- Each film coated tablet contains: Etoricoxib60 mgExcipientsq.s.
Approved colour used in coating.
- Each film coated tablet contains: Etoricoxib90 mgExcipientsq.s.
Colour: Approved colour used
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Each film coated tablet contains:
Ibuprofen BP/USP400 mgParacetamol BP/USP325 mgExcipientsq.s.Colour: Approved colour used in coating.
-
Each film coated tablet contains:
Ibuprofen BP/USP400 mgExcipientsq.s.Approved colours used in coating.
-
Each uncoated tablet contains:
Meloxicam BP/USP15 mgExcipientsq.s. -
Composition:
Menthol USP5.91% w/wEucalyptus oil BP/USP1.97% w/wMethyl Salicylate BP/USP12.80% w/wTurpentine oil BP1.47% w/wCamphor BP/USP1.0% w/wThymol BP/USP0.1% w/wIn an ointment baseq.s. -
Each uncoated tablet contains:
Naproxen BP/USP500 mgExcipientsq.s. -
Each enteric coated tablet contains:
Serratiopeptidase10 mgExcipientsq.s.Colour : Approved colour used
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Each uncoated chewable tablet contains:
Albendazole BP/USP400 mgExcipientsq.s. -
Each film coated tablet contains:
Albendazole BP/USP400 mgExcipientsq.s.Approved colors used in coating.
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Each uncoated tablet contains:
Albendazole USP200 mgExcipientsq.s.Approved colours used.
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Each chewable uncoated tablet contains:
Mebendazole BP/USP100 mgExcipientsq.s. -
Each uncoated tablet contains:
Mebendazole BP/USP100 mgExcipientsq.s. -
Each film coated tablet contains:
Praziquantel BP/USP600 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated tablet contains:
Cetirizine Hydrochloride BP10 mgExcipientsq.s.Colour : Approved Colour used
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Each film coated tablet contains:
Fexofenadine Hydrochloride BP/USP120 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Fexofenadine Hydrochloride BP/USP120 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Fexofenadine Hydrochloride BP/USP180 mgExcipientsq.s.Approved colours used in coating.
- Each film coated tablet contains: Levocetirizine Dihydrochloride USP5 mgExcipientsq.s.
Colour: Approved colour used.
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Each film coated tablet contains:
Montelukast Sodium BP/USP
equivalent to Montelukast10 mgLevocetirizine Hydrochloride USP-5 mg
Excipientsq.s.Colour: Approved colour used
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Each film coated tablet contains:
Azithromycin Dihydrate BP/USP
equivalent to Azithromycin250 mgExcipientsq.s.Colour: Approved colours used
-
Each film coated tablet contains:
Azithromycin Dihydrate BP/USP
equivalent to Azithromycin500 mgExcipientsq.s.Colour: Approved colours used
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Composition:
Chloramphenicol USP1% w/wIn Ointment baseq.s. -
Each film coated tablet contains:
Ciprofloxacin Hydrochloride BP/USP
Eq. to Ciprofloxacin500 mgTinidazole BP/USP600 mgExcipientsq.s.Approved colours used in coating.
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Each film coated tablet contains:
Ciprofloxacin Hydrochloride BP/USP
Equivalent to Ciprofloxacin500 mgOrnidazole500 mgExcipients q.s.
Approved colours used in coatings
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Each film coated tablet contains:
Ciprofloxacin Hydrochloride BP/USP
Eq. to Ciprofloxacin250 mgExcipientsq.s.Approved colours used in coating.
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Each film coated tablet contains:
Ciprofloxacin Hydrochloride BP/USP
Eq. to Ciprofloxacin500 mgExcipientsq.s.Approved colours used in coating.
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Each film coated tablet contains:
Clarithromycin BP/USP500 mgExcipientsq.s.Approved colors used in coating.
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Each hard gelatin capsule contains:
Clindamycin Hydrochloride BP/USP
Eq. to Clindamycin300 mgExcipientsq.s.Approved colors used in empty capsule shells.
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Each uncoated tablet contains:
Trimethoprim BP/USP160 mgSulphamethoxazole BP/USP800 mgExcipientsq.s. -
Each uncoated tablet contains:
Trimethoprim BP/USP80 mgSulphamethoxazole BP/USP400 mgExcipientsq.s. -
Each hard gelatin capsule contains:
Doxycycline Hyclate BP/USP
Eq. to Doxycycline100 mgLactic Acid Bacillus5 billion sporesApproved colours used in empty capsule shells.
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Each hard gelatin capsule contains:
Doxycycline Hyclate BP/USP
Eq. to Doxycycline100 mgExcipientsq.s.Approved colours used in empty capsule shells.
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Each uncoated tablet contains:
Erythromycin Stearate BP/USP
eq. to Erythromycin500 mgExcipientsq.s. -
Each Combikit contains:
(A) One Fluconazole Tablets 150 mg,
Each uncoated tablet contains:
Fluconazole USP150 mgExcipientsq.s.Colour: Ponceau 4R
(B) One Azithromycin Tablet
Each film coated tablet contains:
Azithromycin USP1 gColour: Ponceau 4R
(C) Two Secnidazole Tablets
Each film coated tablet contains:
Secnidazole1 gColour: Titanium Dioxide USP
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Composition:
Gentamicin Sulphate BP/USP
Eq. to Gentamicin base0.1% w/wIn an ointment baseq.s. -
Each gram contains:
Gentamicin Sulphate BP/USP
Eq. to Gentamicin base1% w/wIn an ointment baseq.s. -
Each film coated tablet contains:
Levofloxacin Hemihydrate USP
equivalent to Levofloxacin500 mgExcipientsq.s.Colour: Approved colour used.
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Each film coated tablet contains:
Levofloxacin Hemihydrate USP
equivalent to Levofloxacin750 mgExcipientsq.s.Colour: Approved colour used.
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Each film coated tablet contains:
Linezolid USP600 mgExcipientsq.s.Approved colors used in coating.
- Composition: Metronidazole BP/USP0.75% w/wWater soluble gel baseq.s.
-
Each uncoated tablet contains:
Metronidazole BP/USP250 mgExcipientsq.s. -
Each film coated tablet contains:
Metronidazole BP/USP500 mgExcipientsq.s.Approved colours used in coating.
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Each film coated tablet contains:
Moxifloxacin Hydrochloride BP/USP
equivalent to Moxifloxacin400 mgExcipientsq.s.Approved colors used in coating.
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Composition:
Mupirocin BP/USP2% w/wOintment baseq.s. -
Composition:
Each gram of ointment contains:
Neomycin Sulphate USP3300 IUBacitracin USP250 IUIn an ointment baseq.s. -
Each film coated sustained release tablet contains:
Nitrofurantoin USP100 mgExcipientsq.s.Approved colour used in coating.
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Each film coated tablet contains:
Norfloxacin BP400 mgExcipientsq.s.Colour: Approved colour used.
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Each film coated tablet contains:
Ofloxacin BP/USP200 mgOrnidazole500 mgExcipientsq.s.Colour: Approved colour used.
-
Each film coated tablet contains:
Ofloxacin USP200 mgExcipientsq.s.Colour: Approved colour used
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Each film coated tablet contains:
Ofloxacin USP400 mgExcipientsq.s.Colour: Approved colour used
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Each hard gelatin capsule contains:
Tetracycline Hydrochloride BP/USP500 mgExcipientsq.s.Approved colours used in empty hard gelatin capsule shells.
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Each hard gelatin capsule contains:
Dabigatran Etexilate Mesilate BP
Eq. to Dabigatran Etexilate75 mgExcipientsq.s.Approved colors used in empty capsule shells.
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Each uncoated bilayer tablet contains:
Tranexamic Acid BP/USP635 mg(In Sustained Release Form)
Tranexamic Acid BP/USP115 mg(In Immediate Release Form)
Excipientsq.s.Colour: Approved colour used.
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Each film coated tablet contains:
Tranexamic Acid BP/USP500 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Canagliflozin Hemihydrate
Eq. to Canagliflozin300 mgExcipientsq.s.Approved colors used in coating
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Each film coated tablet contains:
Dapagliflozin Propanediol Monohydrate USP
Eq. to Dapagliflozin10 mgMetformin Hydrochloride BP/USP1000 mg(As extended release)
Excipientsq.s.Approved colours used in coatings
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Each film coated tablet contains:
Dapagliflozin Propanediol Monohydrate USP
Eq. to Dapagliflozin10 mgMetformin Hydrochloride BP/USP500 mg(As extended release)
Excipientsq.s.Approved colours used in coatings
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Each film coated tablet contains:
Dapagliflozin Propanediol Monohydrate USP
Eq. to Dapagliflozin5 mgMetformin Hydrochloride BP/USP1000 mg(As extended release)
Excipientsq.s.Approved colours used in coatings
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Each film coated tablet contains:
Dapagliflozin Propanediol Monohydrate USP
Eq. to Dapagliflozin5 mgMetformin Hydrochloride BP/USP500 mg(As extended release)
Excipientsq.s.Approved colours used in coatings
-
Each film coated tablet contains:
Dapagliflozin Propanediol USP
Equivalent to Dapagliflozin10 mgExcipientsq.s.Colours: Approved color used in coating.
-
Each film coated tablet contains:
Dapagliflozin Propanediol USP
Equivalent to Dapagliflozin5 mgExcipientsq.s.Colours: Approved color used in coating.
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Each film coated tablet contains:
Empagliflozin12.5 mgMetformin Hydrochloride BP/USP1000 mgExcipientsq.sApproved colours used in coating.
-
Each film coated tablet contains:
Empagliflozin12.5 mgMetformin Hydrochloride BP/USP500 mgExcipientsq.sApproved colours used in coating.
-
Each film coated tablet contains:
Empagliflozin5 mgMetformin Hydrochloride BP/USP1000 mgExcipientsq.sApproved colours used in coating.
-
Each film coated tablet contains:
Empagliflozin5 mgMetformin Hydrochloride BP/USP500 mgExcipientsq.sApproved colours used in coating.
-
Each film coated tablet contains:
Empagliflozin10 mgExcipientsq.s.Approved colors used in coating.
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Each film coated tablet contains:
Empagliflozin25 mgExcipientsq.s.Approved colors used in coating.
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Composition:-
Each Film Coated Tablet Contains
Linagliptin5 mgExcipients q.s
Colour: Approved colour used.
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Each film coated bilayered tablet contains:
Metformin Hydrochloride BP500 mg(as Prolonged release)
Sitagliptin Phosphate Monohydrate BP
eq. to Sitagliptin100 mgExcipientsq.s.Approved colours used in coating.
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Each uncoated bilayered tablet contains:
Metformin Hydrochloride BP/USP500 mgRepaglinide BP/USP0.5 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated bilayered tablet contains:
Metformin Hydrochloride BP/USP500 mgRepaglinide BP/USP1 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated bilayered tablet contains:
Metformin Hydrochloride BP/USP500 mgRepaglinide BP/USP2 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated tablet contains:
Metformin Hydrochloride BP500 mgExcipientsq.s. -
Each uncoated tablet contains:
Metformin Hydrochloride BP850 mgExcipientsq.s. -
Each film coated tablet contains:
Metformin Hydrochloride BP/USP500 mgExcipientsq.s.Approved colours used in coating.
-
Each uncoated tablet contains:
Metformin Hydrochloride USP500 mgExcipientsq.s. -
Each uncoated tablet contains:
Metformin Hydrochloride USP850 mgExcipientsq.s. -
Each uncoated tablet contains:
Repaglinide BP/USP0.5 mgVoglibose0.2 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated tablet contains:
Repaglinide BP/USP0.5 mgVoglibose0.3 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated tablet contains:
Repaglinide BP/USP1.0 mgVoglibose0.2 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated tablet contains:
Repaglinide BP/USP1.0 mgVoglibose0.3 mgExcipientsq.s.Colour: Approved colour used.
-
Each uncoated tablet contains:
Repaglinide BP/USP1 mgExcipientsq.s. -
Each uncoated tablet contains:
Repaglinide BP/USP2 mgExcipientsq.s. -
Each film coated tablet contains:
Sitagliptin Phosphate Monohydrate BP
eq. to Sitagliptin50 mgMetformin Hydrochloride BP/USP1000 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Sitagliptin Phosphate Monohydrate BP
eq. to Sitagliptin50 mgMetformin Hydrochloride BP/USP500 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Sitagliptin Phosphate Monohydrate BP
eq. to Sitagliptin100 mgMetformin Hydrochloride BP1000 mg(As sustained release form)
Excipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Sitagliptin Phosphate Monohydrate BP
eq. to Sitagliptin50 mgMetformin Hydrochloride BP850 mg(As sustained release form)
Excipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Sitagliptin Phosphate USP
eq. to Sitagliptin100 mgExcipientsq.s.Approved colours used in coating.
-
Each Film Coated Tablet Contains
Sitagliptin Phosphate USP
Eq.to Sitagliptin25 mgExcipientsq.sColour : Approved colour used.
-
Each film coated tablet contains:
Sitagliptin Phosphate USP
eq. to Sitagliptin50 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Teneligliptin Hydrobromide Hydrate
eq .to Teneligliptin20 mgExcipientsq.s.Approved colors used in coating.
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Each uncoated tablet contains:
Vildagliptin100 mgExcipientsq.s. -
Each uncoated tablet contains:
Vildagliptin50 mgExcipientsq.s. -
Each uncoated Mouth Dissolving tablet contains:
Voglibose0.3 mgExcipientsq.s.
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Composition:
Each gram contains:
Clotrimazole BP/USP1% w/wIn a cream baseq.s. -
Composition:
Each gram contains:
Clotrimazole USP2% w/wIn a cream baseq.s. -
Each hard gelatin capsule contains:
Fluconazole USP150 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Fluconazole BP150 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Fluconazole BP200 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each uncoated tablet contains:
Fluconazole BP/USP150 mgExcipientsq.s. -
Each uncoated tablet contains:
Fluconazole BP/USP200 mgExcipientsq.s.Approved colours used.
-
Each uncoated tablet contains:
Fluconazole BP/USP400 mgExcipientsq.s.Approved colours used.
-
Each uncoated tablet contains:
Griseofulvin BP/USP500 mgExcipientsq.s. -
Each film coated tablet contains:
Itraconazole BP/USP100 mgTerbinafine Hydrochloride BP/USP
Eq. to Terbinafine250 mgExcipientsq.s.Approved colors used in coating.
-
Each hard gelatin capsule contains:
Itraconazole BP/USP130 mgExcipientsq.s.Approved colours used in capsule shells.
-
Each hard gelatin capsule contains:
Itraconazole BP/USP65 mgExcipientsq.s.Approved colours used in capsule shells.
- Each hard gelatin capsule contains: Itraconazole BP/USP100 mg (as pellets)Excipientsq.s.
Approved colour used in empty capsule shells.
- Each hard cellulose capsule contains: Itraconazole BP/USP200 mg
(as pellets)
Excipientsq.s.Approved colours used in empty capsule shells.
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Composition:
Ketoconazole USP2.0% w/wCream baseq.s. - Composition: Luliconazole1.0% w/w
Preservatives:
Benzyl Alcohol USP1% w/wIn cream baseq.s. -
Composition:
Miconazole Nitrate BP/USP2.0% w/wPreservative:
Chlorocresol0.1% w/wIn a cream base with propylene Glycolq.s.Excipientsq.s. -
Composition:
Sertaconazole Nitrate BP2.0% w/wBenzyl Alcohol BP1.0% w/w(As Preservative)
In a cream baseq.s.
-
Each uncoated tablet contains:
Artemether USP20 mgLumefantrine USP120 mgExcipientsq.s. -
Each uncoated tablet contains:
Artemether USP80 mgLumefantrine USP480 mgExcipientsq.s. -
Each film coated tablet contains:
Dihydroartemisinin40 mgPiperaquine Phosphate320 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated tablet contains:
Aceclofenac BP100 mgDrotaverine Hydrochloride80 mgExcipientsq.s.Approved colours used in coating.
-
Each tablet contains:
Drotaverine Hydrochloride40 mgExcipientsq.s. -
Each film coated tablet contains:
Drotaverine Hydrochloride80 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Mebeverine Hydrochloride BP
Equivalent to Mebeverine135 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Mefenamic acid BP/USP250 mgDrotaverine Hydrochloride80 mgExcipientsq.s.Colour: Approved colour used.
-
Composition:
Aciclovir BP5% w/wCream Baseq.s.
-
Each uncoated tablet contains:
Amlodipine Besilate USP
Eq. to Amlodipine10 mgExcipientsq.s. -
Each film coated tablet contains:
Amlodipine Besilate BP/USP
Eq. to Amlodipine10 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Amlodipine Besilate BP/USP
Eq. to Amlodipine5 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Carvedilol BP/USP6.25 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Clopidogrel Bisulphate USP
Eq. to Clopidogrel75 mgExcipientsq.s. -
Each uncoated tablet contains:
Enalapril Maleate BP/USP2.5 mgExcipientsq.s. -
Each uncoated tablet contains:
Enalapril Maleate BP/USP5 mgExcipientsq.s. -
Each uncoated tablet contains:
Enalapril Maleate USP20 mgExcipientsq.s. -
Each uncoated tablet contains:
Furosemide BP/USP40 mgExcipientsq.s. -
Each uncoated tablet contains:
Hydrochlorothiazide BP/USP25 mgExcipientsq.s. -
Each film coated tablet contains:
Losartan Potassium USP100 mgHydrochlorothiazide USP25 mgExcipientsq.s.Colours: Approved colours used in coaing.
Each film coated tablet contains:
Rosuvastatin calcium BP/USP
Eq. to Rosuvastatin10 mgEzetimibe USP10 mgExcipientsq.s.Colours: Approved colours used
-
Each film coated tablet contains:
Losartan Potassium BP/USP50 mgExcipientsq.s.Approved colours used in coating.
-
Each extended – release film coated tablet contains:
Nifedipine BP/USP10 mgExcipientsq.s.Approved colour used in coating.
-
Each extended – release film coated tablet contains:
Nifedipine BP/USP60 mgExcipientsq.s.Approved colour used in coating.
-
Each extended – release film coated tablet contains:
Nifedipine USP20 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Sacubitril Sodium
Eq. to Sacubitril49 mgValsartan BP/USP51 mgExcipientsq.s.Colour: Approved colour used in coating.
-
Each film coated tablet contains:
Sacubitril Sodium
Eq. to Sacubitril24 mgValsartan BP/USP26 mgExcipients q.s.
Colour: Approved colour used in coating
-
Each film coated tablet contains:
Sacubitril Sodium
Eq. to Sacubitril97 mgValsartan BP/USP103 mgExcipients q.s.
Colour: Approved colour used in coating
-
Each uncoated tablet contains:
Telmisartan USP80 mgHydrochlorothiazide BP12.5 mgExcipientsq.s. -
Each uncoated tablet contains:
Telmisartan BP/USP40 mgExcipientsq.s. -
Each uncoated tablet contains:
Telmisartan BP/USP80 mgExcipientsq.s. -
Each uncoated tablet contains:
Torsemide USP10 mgExcipientsq.s. -
Each uncoated tablet contains:
Torsemide USP5 mgExcipientsq.s. -
Each film coated tablet contains:
Valsartan BP/USP160 mgHydrochlorothiazide BP/USP12.5 mgExcipientsq.s.Approved colours used.
-
Each film coated tablet contains:
Valsartan BP/USP80 mgHydrochlorothiazide BP/USP12.5 mgExcipientsq.s.Approved colours used.
-
Each uncoated tablet contains
Dexamethasone BP/USP0.5 mgExcipientsq.s. -
Each uncoated tablet contains:
Dexamethasone BP/USP6 mgExcipientsq.s. -
Each uncoated tablet contains:
Hydrocortisone USP10 mgExcipientsq.s. -
Each film coated tablet contains:
Methylprednisolone BP/USP16 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Methylprednisolone BP/USP8 mgExcipientsq.s.Approved colour used in coating.
-
Each uncoated tablet contains:
Prednisolone BP/USP10 mgExcipientsq.s. -
Each uncoated tablet contains:
Prednisolone BP/USP5 mgExcipientsq.s.
-
Composition:
Benzoyl Peroxide BP
Eq. to Anhydrous Benzoyl Peroxide5% w/wGel Baseq.s. -
Composition:
Betamethasone Valerate USP
eq. to Betamethasone0.1% w/wGentamicin Sulphate USP
eq. to Gentamycin base0.1% w/wMiconazole Nitrate USP2.0% w/wChlorocresol (as preservative) USP- 0.1% w/w
Cream Baseq.s. -
Composition:
Calcium Dobesilate Monohydrate BP
eq.to Calcium Dobesilate0.25% w/wLignocaine Hydrochloride BP/USP
eq. to Anhydrous Lignocaine3% w/wHydrocortisone Acetate BP/USP - 0.25% w/w
Zinc (as Zinc Oxide BP/USP)5% w/wIn cream baseq.s. -
Composition:
Clindamycin Phosphate BP/USP
Eq. to Clindamycin1% w/wAdapalene BP/USP0.1% w/wGel Baseq. s -
Composition:
Clindamycin Phosphate BP/USP
Eq. to Clindamycin1.00% w/wPreservatives
Sodium Methylparaben USP0.10% w/wSodium Propylparaben USP0.05% w/wGel baseq.s -
Composition:
Clobetasol Propionate USP0.05 % w/wSalicylic Acid USP3.00 % w/wOintment baseq.s. -
Compositions:
Clobetasol Propionate BP/USP0.05% w/wIn a cream baseq.s. -
Compositions:
Clobetasol Propionate BP/USP - 0.05% w/w
Miconazole Nitrate BP/USP2.0% w/wNeomycin Sulphate BP/USP
equivalent to Neomycin0.5% w/wIn a cream baseq.s. -
Compositions:
Clobetasol Propionate BP/USP0.05% w/wMiconazole Nitrate BP/USP2.0% w/wNeomycin Sulphate BP
equivalent to Neomycin0.5% w/wZinc oxide BP/USP2.5% w/wBorax BP0.05% w/wChlorocresol BP0.1% w/w(as a Preservative)
In a cream baseq.s. -
Compositions:
Clobetasol Propionate BP0.05% w/wOfloxacin BP0.75% w/wOrnidazole2% w/wItraconazole BP1% w/wMethylparaben BP0.2% w/w(as preservative)
Propylparaben BP0.2% w/w(as preservative)
In a cream baseq.s.. -
Compositions:
Betamethasone Dipropionate BP-0.05% w/w
Clotrimazole BP/USP1.0% w/wIn a cream baseq.s. -
Composition:
Hydrocortisone BP/USP1.0% w/wIn a cream baseq.s. -
Composition:
Hydrocortisone acetate BP/USP1% w/wIn an ointment baseq.s. -
Compositions:
Ketoconazole BP/USP2.0% w/wIodochlorhydroxyquinoline1.0% w/wTolnaftate BP/USP1.0% w/wNeomycin Sulphate BP/USP
equivalent to Neomycin0.1% w/wClobetasol Propionate BP/USP0.05% w/wChlorocresol (as preservative) BP-0.1% w/w
Cream baseq.s. -
Composition:
Lignocaine Hydrochloride BP/USP2.0% w/wIn a gel baseq.s. -
Composition
Minoxidil USP/BP5% w/vIsopropyl Alcohol USP/BPq.s. -
Composition:
Mometasone Furoate BP/USP0.1 % w/wTretinoin USP0.025 % w/wHydroquinone BP/USP2.0 % w/wIn a cream baseq.s. -
Each gram contains:
Oxytetracycline Hydrochloride BP/USP25,800 IUHydrocortisone Acetate BP/USP10 mgIn an ointment baseq.s.
-
Each film coated tablet contains:
Dapoxetine Hydrochloride
Equivalent to Dapoxetine30 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Sildenafil Citrate BP/USP
equivalent to Sildenafil100 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Tadalafil BP/USP10 mgDapoxetine Hydrochloride
Eq. to Dapoxetine30 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Tadalafil BP/USP20 mgDapoxetine Hydrochloride
Eq. to Dapoxetine30 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Tadalafil BP/USP20 mgDapoxetine Hydrochloride
Eq. to Dapoxetine60 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Tadalafil BP/USP20 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Acotiamide Hydrochloride Hydrate100 mgExcipientsq.s.Approved colours used in coating.
-
Dexrabeprazole Sodium 10 mg
Domperidone BP 30 mg
-
Each hard gelatin capsule contains:
Esomeprazole Magnesium Trihydrate BP
Eq. to Esomeprazole40 mg(as enteric coated pellets)
Domperidone BP30 mg(as sustained release pellets)
Excipientsq.s.Approved colours used in empty capsule shells.
-
Esomeprazole Magnesium Trihydrate BP eq. to Esomeprazole 40 mg
Levosulpiride 75 mg
-
Each film coated tablet contains:
Famotidine BP/USP40 mgExcipientsq.s.Approved colours used.
-
Each uncoated mouth dissolving tablet contains:
Lansoprazole BP/USP15 mgExcipientsq.s. -
Each hard gelatin capsule contains:
Omeprazole BP20 mg(as enteric coated pellets)
Domperidone BP30 mg(as sustained release pellets)
Excipientsq.s.Approved colours used in capsule shells.
-
Each hard gelatin capsule contains:
Omeprazole BP/USP20 mg(As enteric coated granules)
Excipientsq.s.Approved colours used in empty capsule shells.
-
Each film coated Tablet Contains:
Ondansetron Hydrochloride Dihydrate BP
Eq. to Ondansetron8 mgExcipientsq.s.Colour :approved colour used -
Each orally disintegrating tablet contains:
Ondansetron Hydrochloride USP
Eq. to Ondansetron8 mgExcipientsq.s. -
Each hard gelatin capsule contains:
Pancreatin USP300 mg(As enteric coated form)
Equivalent to
Lipase Activity25000 Ph. Eur UnitsAmylase Activity20000 Ph. Eur UnitsProtease Activity1000 Ph. Eur UnitsExcipientsq.s.Approved colours used in empty capsule shells.
-
Each enteric coated tablet contains:
Pancreatin BP/USP170 mgActivated Dimethicone USP80 mgFructooligosaccharide100 mgExcipientsq.s.Approved colours used in coating.
-
Each enteric coated tablet contains:
Pancreatin BP170 mgActivated Dimethicone BP80 mgFructooligosaccharide100 mgExcipientsq.s.Approved colors used in coating.
-
Each enteric coated tablet contains:
Pantoprazole Sodium Sesquihydrate BP
equivalent to Pantoprazole40 mgDomperidone BP
Equivalent to Domperidone10 mgExcipientsq.s.Approved colours used in coating.
-
Each hard gelatin capsule contains:
Pantoprazole Sodium Sesquihydrate BP/USP equivalent to Pantoprazole40 mg (Gastro-resistant form)Domperidone BP30 mg(Prolonged-release form)
Excipientsq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each hard gelatin capsule contains:
Pantoprazole Sodium Sesquihydrate BP/USP equivalent to Pantoprazole40 mg (Gastro-resistant form)Itopride Hydrochloride150 mg(as sustained-release form)
Excipientsq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each enteric coated tablet contains:
Pantoprazole Sodium Sesquihydrate
BP/USP
equivalent to Pantoprazole40 mgExcipientsq.s.Approved colours
used in coating.
-
Each enteric coated tablet contains:
Pantoprazole Sodium USP20 mgExcipientsq.s.Colour : Approved colour used
-
Each hard gelatin capsule contains:
Rabeprazole Sodium BP20 mg(as gastro-resistant form)
Domperidone BP30 mg(as sustained-release form)
Excipientsq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each hard gelatin capsule contains:
Rabeprazole Sodium BP/USP20 mg(as enteric coated form)
Levosulpiride75 mg(as sustained release form)
Excipientsq.s.Approved colours used in empty hard gelatin capsule shells.
-
Each film coated tablet contains:
Ranitidine Hydrochloride BP/USP
equivalent to Ranitidine150 mgExcipientsq.s.Colour: Approved colour used
-
Each film coated tablet contains:
Ranitidine Hydrochloride USP
equivalent to Ranitidine300 mgExcipientsq.s.Colour: Approved colour used
-
Each uncoated tablet contains:
Ursodeoxycholic Acid BP / USP150 mgExcipientsq.s. -
Each hard gelatin capsule contains:
Ursodeoxycholic Acid BP450 mgExcipientsq.s.Approved colours used in capsule shells.
-
Each film coated sustained -release tablet contains:
Ursodeoxycholic Acid BP300 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated sustained -release tablet contains:
Ursodeoxycholic Acid BP600 mgExcipientsq.s.Approved colors used in coating.
- Each uncoated tablet contains: Ursodeoxycholic Acid BP300 mgExcipientsq.s.
-
Each uncoated tablet contains:
Ursodeoxycholic Acid BP600 mgExcipientsq.s.
-
Each uncoated tablet contains:
Misoprostol BP/USP100 mcgExcipientsq.s. -
Each uncoated tablet contains:
Misoprostol BP/USP200 mcgExcipientsq.s. -
Each uncoated tablet contains:
Misoprostol BP/USP25 mcgExcipientsq.s. -
Each uncoated tablet contains:
Misoprostol BP/USP50 mcgExcipientsq.s. -
Each uncoated tablet contains:
Misoprostol BP/USP600 mcgExcipientsq.s. -
Each film coated tablet contains:
Myo-Inositol1000 mgCholecalciferol BP/USP2000 IUChromium Picolinate USP100 mcgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Atorvastatin Calcium BP/USP
eq. to Atorvastatin20 mgExcipientsq.s.Approved colours used in coating.
-
Rosuvastatin Calcium BP/USP eq. to Rosuvastatin 10 mg
Ezetimibe USP 10 mg
-
Each film coated tablet contains:
Rosuvastatin Calcium BP/USP
equivalent to Rosuvastatin10 mgFenofibrate BP/USP160 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium BP
eq. to Rosuvastatin10 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium BP
eq. to Rosuvastatin20 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium BP
eq. to Rosuvastatin40 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium BP
Eq. to Rosuvastatin5 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium USP
Eq. to Rosuvastatin10 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium USP
eq. to Rosuvastatin20 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Rosuvastatin Calcium USP
Eq. to Rosuvastatin5 mgExcipientsq.s.Approved colors used in coating.
-
Each uncoated Chewable tablet contains:
Ascorbic Acid BP/USP100 mgSodium Ascorbate USP450 mgeq. to Ascorbic acid400 mgZinc Citrate USP
eq to elemental zinc5 mgExcipientsq.s. -
Each film coated tablet contains:
Calcitriol USP0.25 mcgExcipients q.s.
-
Each film coated tablet Contains:
1250mg
Calcium Carbonate
From an Organic Source
(Powdered Oyster Shell) Equivalent to
Elemental Calcium500 mgVitamin D3 250IU
Color: Approved colors used in coating
-
Each film coated tablet contains:
1.25 g of Calcium Carbonate BP/USP from an organic source (Oyster Shell) equivalent to elemental Calcium500 mgVitamin D3 BP/USP250 IUExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Calcium Carbonate BP/USP1.25 gEq. to elemental Calcium500 mgCholecalciferol BP/USP250 IUExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
Calcium Carbonate BP/USP
equivalent to elemental Calcium— 500 mg
Calcitriol BP/USP0.25 mcgVitamin K2 7100 mcgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Calcium Carbonate BP/USP1250 mgEq. to Elemental Calcium500 mgVitamin D3 BP/USP2000 IUMethylcobalamin USP1500 mcgL-Methylfolate Calcium1 mgPyridoxal-5-Phosphate20 mgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Calcium Citrate Malate USP
eq. to Elemental Calcium250 mgCalcitriol BP/USP0.25 mcgVitamin K2 7580 mcgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Calcium Citrate Malate USP
equivalent to elemental Calcium250 mgCalcitriol BP/USP0.25 mcgFolic Acid BP/USP100 mcgZinc Sulphate BP/ USP7.5 mgVitamin K2 750 mcgExcipientsq.s.Approved colours used in coating.
-
Each film coated tablet contains:
Calcium Citrate USP1000 mgVitamin D3 BP/USP200 IUMagnesium Hydroxide BP
equivalent to Magnesium100 mgZinc Sulphate (Monohydrate) BP
equivalent to elemental Zinc4 mgExcipientsq.s.Approved colors used in coating.
-
Each uncoated tablet contains:
Folic acid BP/USP5 mgExcipientsq.s. -
Each hard gelatin capsule contains:
Iron (III) Hydroxide Polymaltose Complex equivalent to elemental Iron100 mgFolic Acid BP/USP550 mcgExcipientsq.s.Appropriate overages of Vitamin added.
Approved colours used in the capsule shells.
-
Each film coated tablet contains:
L-Methylfolate Calcium1 mgPyridoxal-5-Phosphate0.5 mgMethylcobalamin USP1500 mcgExcipientsq.s.Approved colour used in coating.
-
Each uncoated sublingual tablet contains:
Mecobalamin1500 mcgExcipientsq.s. -
Each uncoated tablet contains:
Vitamin D3 BP/USP2000 IUVitamin K2 750 mcgExcipientsq.s. -
Each film coated tablet contains:
Zinc Acetate USP
Eq. to elemental Zinc10 mgExcipients q.s.
-
Each uncoated tablet contains:
Zinc Sulphate Monohydrate BP/USP
Eq. to Elemental Zinc20 mgExcipientsq.s. -
Each film coated tablet contains:
Zinc Sulphate Monohydrate BP/USP
Eq. to Elemental Zinc10 mgExcipientsq.s.Colour: Approved colour used
-
Each film coated tablet contains:
Gabapentin BP/USP100 mgMethylcobalamin USP500 mcgExcipientsq.s.Approved colors used in coating.
-
Each hard gelatin capsule contains:
Gabapentin USP300 mgExcipientsq.s.Approved colors used in coating.
-
Each film coated tablet contains:
L-Carnitine L-Tartrate
Eq. to L-Carnitine500 mgMethylcobalamin USP1500 mcgFolic Acid BP/USP1.5 mgExcipientsq.s.Approved colour used in coating.
-
Each film coated tablet contains:
L-Carnitine L-Tartrate
Eq. to L-Carnitine500 mgMethylcobalamin USP500 mcgFolic Acid BP/USP1.5 mgExcipientsq.s.Approved colour used in coating.
-
Each Film coated Sustained Release tablet Contains:
Levetiracetam USP/BP500 mgExcipients q.s.
Colour: Approved Colour used in coating
-
Each film coated tablet contains:
Levetiracetam USP500 mgExcipientsq.s.Approved colors used in coating.
-
Each hard gelatin capsule contains:
Mecobalamin1500 mcgFolic Acid BP/USP1.5 mgPyridoxine Hydrochloride BP/USP3 mgAlpha Lipoic Acid USP100 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Pregabalin BP/USP75 mgMethylcobalamin USP750 mcgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Pregabalin BP/USP150 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Pregabalin BP/USP300 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each hard gelatin capsule contains:
Pregabalin BP/USP75 mgExcipientsq.s.Approved colours used in empty capsule shells.
-
Each enteric coated tablet contains:
Duloxetine Hydrochloride BP/USP
Eq. to Duloxetine30 mgExcipientsq.s.Approved colors used in coating.
-
Each hard gelatin capsule contains:
Duloxetine Hydrochloride USP30 mgExcipientsq.s.Approved colours used in capsule shells.
-
Each hard gelatin capsule contains:
Duloxetine Hydrochloride USP60 mgExcipientsq.s.Approved colours used in capsule shells.
-
Each film coated tablet contains:
Eacitalopram Oxalate BP Eq. to
Escitalopram10 mgExcipients q.s.
Approved colour used in coating.
-
Each film coated tablet contains:
Eacitalopram Oxalate BP Eq. to
Escitalopram20 mgExcipients q.s.
Approved colour used in coating.
-
Each Film coated Tablet Contains:
Risperidone USP/BP2 mgExcipients q.s.
Colour: Approved colours used in coating
-
Each hard gelatin Capsule contains:
Silodosin4 mgDutasteride BP/USP0.5 mg(As Pellets form)
Colours: Approved colours used in Empty capsule shells.
-
Each hard gelatin Capsule contains:
Silodosin8 mgDutasteride BP/USP0.5 mg(As Pellets form)
Colours: Approved colours used in Empty capsule shells.
-
Each film coated tablet contains:
Tamsulosin Hydrochloride BP/USP0.4 mg(As modified release)
Dutasteride BP/USP0.5 mgExcipientsq.s.Colour: Approved colour used in coating.
- Each film coated tablet contains: Febuxostat40 mgExcipientsq.s.
Colour: Approved colour used.
- Each film coated tablet contains: Febuxostat80 mgExcipientsq.s.
Colour: Approved colour used
-
Each film coated tablet contains:
Sevelamer Hydrochloride400 mgExcipientsq.s.Colours:approved colours used -
Each film coated tablet contains:
Sevelamer Hydrochloride800 mgExcipientsq.s.Colours:approved colours used -
Each hard gelatin capsule contains:
Tacrolimus USP0.25 mgExcipientq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each hard gelatin prolong release capsule contains:
Tacrolimus USP0.5 mgExcipientq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each hard gelatin prolong release capsule contains:
Tacrolimus USP1 mgExcipientq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
-
Each hard gelatin prolong release capsule contains:
Tacrolimus USP5 mgExcipientq.s.Colour: Approved colours used in empty hard gelatin capsule shells.
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