FDA NDC Directory · JSON-LD · Markdown

Mycophenolate Mofetil

NDC 60687-494 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA065410
Dosage form / routeCAPSULE · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (250 mg/1)
Marketing started20200221
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).