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Nipent

NDC 0409-0801 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic namePENTOSTATIN
Labeler / ManufacturerHospira, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020122
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsPENTOSTATIN (2 mg/mL)
Marketing started20070815
Package count1

External sources

Source: openFDA. Public-domain (CC0).