FDA NDC Directory · JSON-LD · Markdown

Myfortic

NDC 0078-0385 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namemycophenolic acid
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA050791
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsMYCOPHENOLATE SODIUM (180 mg/1)
Marketing started20040227
Package count1

External sources

Source: openFDA. Public-domain (CC0).