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Everolimus

NDC 70377-071 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameeverolimus
Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216140
Dosage form / routeTABLET · ORAL
Active ingredientsEVEROLIMUS (.75 mg/1)
Marketing started20250602
Package count2

External sources

Source: openFDA. Public-domain (CC0).