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Amiodarone Hydrochloride

NDC 65219-643 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameAMIODARONE HYDROCHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075761
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsAMIODARONE HYDROCHLORIDE (50 mg/mL)
Marketing started20250505
Package count1

External sources

Source: openFDA. Public-domain (CC0).