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: A076608
Product Number: 001
Approval Date: Dec 3, 2004
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information