FDA NDC Directory · JSON-LD · Markdown

Amiodarone Hydrochloride

NDC 51672-4055 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075424
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (100 mg/1)
Marketing started20010330
Package count1

External sources

Source: openFDA. Public-domain (CC0).