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Amiodarone hydrochloride

NDC 65841-631 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA079029
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (200 mg/1)
Marketing started20090810
Package count5

External sources

Source: openFDA. Public-domain (CC0).