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Everolimus

NDC 72319-003 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameeverolimus
Labeler / Manufactureri3 Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219464
Dosage form / routeTABLET · ORAL
Active ingredientsEVEROLIMUS (.25 mg/1)
Marketing started20260807
Package count2

External sources

Source: openFDA. Public-domain (CC0).