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Quinapril

NDC 65862-620 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameQuinapril Hydrochloride
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202725
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsQUINAPRIL HYDROCHLORIDE (40 mg/1)
Marketing started20130429
Package count5

External sources

Source: openFDA. Public-domain (CC0).