FDA NDC Directory · JSON-LD · Markdown

Amlodipine Besylate

NDC 51655-586 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAmlodipine besylate
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078925
Dosage form / routeTABLET · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
Marketing started20230103
Package count1

External sources

Source: openFDA. Public-domain (CC0).