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Mitomycin

NDC 68001-389 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA064144
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsMITOMYCIN (5 mg/10mL)
Marketing started20190514
Package count1

External sources

Source: openFDA. Public-domain (CC0).