FDA NDC Directory · JSON-LD · Markdown

Mycophenolate Mofetil

NDC 67877-225 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091249
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (500 mg/1)
Marketing started20111128
Package count4

External sources

Source: openFDA. Public-domain (CC0).