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Furosemide

NDC 81565-201 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameFUROSEMIDE
Labeler / ManufacturerPhlow Corporation
Marketing categoryNew Drug Application (innovator) · App NDA018902
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsFUROSEMIDE (10 mg/mL)
Marketing started20220201
Package count1

External sources

Source: openFDA. Public-domain (CC0).