FDA NDC Directory · JSON-LD · Markdown

AMLODIPINE BESYLATE 10 mg

NDC 82804-971 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAMLODIPINE BESYLATE
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA078414
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
Marketing started20211001
Package count7

External sources

Source: openFDA. Public-domain (CC0).