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Ibutilide Fumarate

NDC 23155-326 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204146
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsIBUTILIDE FUMARATE (1 mg/10mL)
Marketing started20240401
Package count1

External sources

Source: openFDA. Public-domain (CC0).