FDA NDC Directory · JSON-LD · Markdown

Amlodipine and Benazepril Hydrochloride

NDC 50090-6770 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA202239
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
BENAZEPRIL HYDROCHLORIDE (10 mg/1)
Marketing started20120905
Package count1

External sources

Source: openFDA. Public-domain (CC0).