FDA NDC Directory · JSON-LD · Markdown

Amiodarone Hydrochloride

NDC 51672-4056 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076362
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (300 mg/1)
Marketing started20031202
Package count3

External sources

Source: openFDA. Public-domain (CC0).