FDA NDC Directory · JSON-LD · Markdown

PLERIXAFOR

NDC 70710-1208 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameplerixafor
Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208980
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsPLERIXAFOR (24 mg/1.2mL)
Marketing started20230728
Package count1

External sources

Source: openFDA. Public-domain (CC0).