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Fludarabine Phosphate

NDC 42658-024 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA220196
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsFLUDARABINE PHOSPHATE (25 mg/mL)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).