FDA NDC Directory · JSON-LD · Markdown

Cyclophosphamide

NDC 68001-442 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Generic namecyclophosphamide
Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA040745
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS ORAL
Active ingredientsCYCLOPHOSPHAMIDE (500 mg/25mL)
Marketing started20201019
Package count1

External sources

Source: openFDA. Public-domain (CC0).