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QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE

NDC 65862-162 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078450
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
QUINAPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20070824
Package count2

External sources

Source: openFDA. Public-domain (CC0).