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Amlodipine Besylate and Benazepril Hydrochloride

NDC 51655-201 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077183
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
BENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20230419
Package count1

External sources

Source: openFDA. Public-domain (CC0).