FDA NDC Directory · JSON-LD · Markdown

Mycophenolate Mofetil

NDC 70752-294 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerQUAGEN PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214525
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (200 mg/mL)
Marketing started20260806
Package count1

External sources

Source: openFDA. Public-domain (CC0).