FDA NDC Directory · JSON-LD · Markdown

Cladribine

NDC 42658-010 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210856
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsCLADRIBINE (1 mg/mL)
Marketing started20200518
Package count1

External sources

Source: openFDA. Public-domain (CC0).