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Amlodipine Besylate and Benazepril Hydrochloride

NDC 72789-502 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078466
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
BENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20180801
Package count1

External sources

Source: openFDA. Public-domain (CC0).