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Everolimus

NDC 0054-0604 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206133
Dosage form / routeTABLET · ORAL
Active ingredientsEVEROLIMUS (1 mg/1)
Marketing started20211118
Package count1

External sources

Source: openFDA. Public-domain (CC0).