FDA NDC Directory · JSON-LD · Markdown

MYCOPHENOLATE MOFETIL

NDC 72603-751 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Generic namemycophenolate mofetil
Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218227
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (200 mg/mL)
Marketing started20260301
Package count1

External sources

Source: openFDA. Public-domain (CC0).