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Sirolimus

NDC 67877-746 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214753
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIROLIMUS (.5 mg/1)
Marketing started20210313
Package count4

External sources

Source: openFDA. Public-domain (CC0).