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mycophenolic acid

NDC 85972-161 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerStellon Biotech Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211173
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsMYCOPHENOLATE SODIUM (180 mg/1)
Marketing started20260911
Package count1

External sources

Source: openFDA. Public-domain (CC0).