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Amlodipine and Benazepril Hydrochloride

NDC 23155-920 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091431
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
BENAZEPRIL HYDROCHLORIDE (10 mg/1)
Marketing started20251219
Package count3

External sources

Source: openFDA. Public-domain (CC0).