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Clofarabine

NDC 70121-1236 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208857
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsCLOFARABINE (1 mg/mL)
Marketing started20171106
Package count1

External sources

Source: openFDA. Public-domain (CC0).