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Furosemide

NDC 70121-1076 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207552
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsFUROSEMIDE (100 mg/10mL)
Marketing started20160725
Package count1

External sources

Source: openFDA. Public-domain (CC0).