FDA NDC Directory · JSON-LD · Markdown

Cladribine

NDC 63323-140 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameCLADRIBINE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076571
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsCLADRIBINE (1 mg/mL)
Marketing started20041201
Package count1

External sources

Source: openFDA. Public-domain (CC0).