FDA NDC Directory · JSON-LD · Markdown

mycophenolate mofetil

NDC 67877-266 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200197
Dosage form / routeCAPSULE · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (250 mg/1)
Marketing started20100101
Package count4

External sources

Source: openFDA. Public-domain (CC0).