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mycophenolate mofetil

NDC 0904-7466 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA200197
Dosage form / routeCAPSULE · ORAL
Active ingredientsMYCOPHENOLATE MOFETIL (250 mg/1)
Marketing started20251211
Package count1

External sources

Source: openFDA. Public-domain (CC0).