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Amiodarone hydrochloride

NDC 68083-112 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077161
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsAMIODARONE HYDROCHLORIDE (50 mg/mL)
Marketing started20130715
Package count1

External sources

Source: openFDA. Public-domain (CC0).