FDA NDC Directory · JSON-LD · Markdown

Mozobil

NDC 0024-5862 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namePLERIXAFOR
Labeler / ManufacturerSanofi-Aventis U.S. LLC
Marketing categoryNew Drug Application (innovator) · App NDA022311
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsPLERIXAFOR (24 mg/1.2mL)
Marketing started20130901
Package count1

External sources

Source: openFDA. Public-domain (CC0).