FDA NDC Directory · JSON-LD · Markdown

Mycophenolate Mofetil

NDC 65050-2073 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerWuxi Fortune Pharmaceutical Co.,Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA214079
Dosage form / routeCAPSULE · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (250 mg/1)
Marketing started20251110
Package count1

External sources

Source: openFDA. Public-domain (CC0).