FDA NDC Directory · JSON-LD · Markdown

AMLODIPINE BESYLATE

NDC 72189-162 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA078925
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (2.5 mg/1)
Marketing started20210112
Package count1

External sources

Source: openFDA. Public-domain (CC0).