FDA NDC Directory · JSON-LD · Markdown

Cladribine

NDC 62049-286 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGenvion Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA218425
Dosage form / routeTABLET · ORAL
Active ingredientsCLADRIBINE (10 mg/1)
Marketing started20251125
Package count7

External sources

Source: openFDA. Public-domain (CC0).