FDA NDC Directory · JSON-LD · Markdown

MYCOPHENOLATE MOFETIL

NDC 64380-899 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212634
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (200 mg/mL)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).