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Amiodarone Hydrochloride

NDC 70436-232 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameamiodarone hydrochloride
Labeler / ManufacturerSlate Run Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA218253
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsAMIODARONE HYDROCHLORIDE (50 mg/mL)
Marketing started20241031
Package count3

External sources

Source: openFDA. Public-domain (CC0).