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amiodarone hydrochloride

NDC 48433-154 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSafecor Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079029
Dosage form / routeTABLET · ORAL
Active ingredientsAMIODARONE HYDROCHLORIDE (200 mg/1)
Marketing started20260601
Package count1

External sources

Source: openFDA. Public-domain (CC0).