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Amiodarone Hydrochloride

NDC 70518-3439 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078578
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (200 mg/1)
Marketing started20220614
Package count2

External sources

Source: openFDA. Public-domain (CC0).