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Amlodipine Besylate and Benazepril Hydrochloride

NDC 55111-587 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090149
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
BENAZEPRIL HYDROCHLORIDE (40 mg/1)
Marketing started20110705
Package count3

External sources

Source: openFDA. Public-domain (CC0).