FDA NDC Directory · JSON-LD · Markdown

Quinapril

NDC 69097-842 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078457
Dosage form / routeTABLET · ORAL
Active ingredientsQUINAPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20160722
Package count2

External sources

Source: openFDA. Public-domain (CC0).