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Bleomycin

NDC 63323-136 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameBLEOMYCIN SULFATE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065185
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAPLEURAL INTRAVENOUS SUBCUTANEOUS
Active ingredientsBLEOMYCIN SULFATE (15 [USP'U]/1)
Marketing started20090213
Package count1

External sources

Source: openFDA. Public-domain (CC0).