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Furosemide

NDC 23155-473 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203428
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsFUROSEMIDE (10 mg/mL)
Marketing started20140902
Package count5

External sources

Source: openFDA. Public-domain (CC0).