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Amlodipine Besylate and Benazepril Hydrochloride

NDC 69238-2684 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077215
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
BENAZEPRIL HYDROCHLORIDE (10 mg/1)
Marketing started20260414
Package count1

External sources

Source: openFDA. Public-domain (CC0).