Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 076739

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FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE (FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE)
10MG;12.5MG
Marketing Status: Discontinued

Active Ingredient: FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Proprietary Name: FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG;12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076739
Product Number: 001
Approval Date: Dec 17, 2004
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE (FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE)
20MG;12.5MG
Marketing Status: Discontinued

Active Ingredient: FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Proprietary Name: FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG;12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076739
Product Number: 002
Approval Date: Dec 17, 2004
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information