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Furosemide

NDC 72789-032 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefurosemide
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076796
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (40 mg/1)
Marketing started20040326
Package count2

External sources

Source: openFDA. Public-domain (CC0).