FDA NDC Directory · JSON-LD · Markdown

amlodipine besylate

NDC 52605-043 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPOLYGEN PHARMACEUTICALS INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA207821
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
Marketing started20160711
Package count2

External sources

Source: openFDA. Public-domain (CC0).