FDA NDC Directory · JSON-LD · Markdown

Quinapril

NDC 63629-7934 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameQuinapril Hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA202725
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsQUINAPRIL HYDROCHLORIDE (10 mg/1)
Marketing started20130429
Package count1

External sources

Source: openFDA. Public-domain (CC0).