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Everolimus

NDC 51991-823 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBreckenridge Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205426
Dosage form / routeTABLET · ORAL
Active ingredientsEVEROLIMUS (7.5 mg/1)
Marketing started20210305
Package count2

External sources

Source: openFDA. Public-domain (CC0).