FDA NDC Directory · JSON-LD · Markdown

Amlodipine Besylate and Benazepril Hydrochloride

NDC 50090-5137 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA077183
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
BENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20100419
Package count2

External sources

Source: openFDA. Public-domain (CC0).