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amiodarone hydrochloride

NDC 68382-298 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079029
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (400 mg/1)
Marketing started20230209
Package count1

External sources

Source: openFDA. Public-domain (CC0).