FDA NDC Directory · JSON-LD · Markdown

Quinapril and Hydrochlorothiazide 20/25

NDC 69097-831 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201356
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (25 mg/1)
QUINAPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20160720
Package count1

External sources

Source: openFDA. Public-domain (CC0).