FDA NDC Directory · JSON-LD · Markdown

CYCLOPHOSPHAMIDE

NDC 68001-565 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namecyclophosphamide
Labeler / ManufacturerBluePoint Laboratories
Marketing categoryNew Drug Application (innovator) · App NDA212501
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsCYCLOPHOSPHAMIDE ANHYDROUS (200 mg/mL)
Marketing started20230410
Package count1

External sources

Source: openFDA. Public-domain (CC0).