FDA NDC Directory · JSON-LD · Markdown

Mycophenolate Mofetil

NDC 42023-172 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic namemycophenolate mofetil
Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203575
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/20mL)
Marketing started20161028
Package count1

External sources

Source: openFDA. Public-domain (CC0).