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Amiodarone Hydrochloride

NDC 55154-3365 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075424
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (200 mg/1)
Marketing started20010330
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).