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Amlodipine and Benazepril Hydrochloride

NDC 84677-013 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091431
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
BENAZEPRIL HYDROCHLORIDE (40 mg/1)
Marketing started20131230
Package count1

External sources

Source: openFDA. Public-domain (CC0).