FDA NDC Directory · JSON-LD · Markdown

sirolimus

NDC 60687-902 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA201676
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIROLIMUS (.5 mg/1)
Marketing started20260602
Package count1

External sources

Source: openFDA. Public-domain (CC0).