"0008-1041-10" National Drug Code (NDC)

NDC Code	0008-1041-10
Package Description	100 BLISTER PACK in 1 CARTON (0008-1041-10) / 1 TABLET, SUGAR COATED in 1 BLISTER PACK
Product NDC	0008-1041
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Rapamune
Non-Proprietary Name	Sirolimus
Dosage Form	TABLET, SUGAR COATED
Usage	ORAL
Start Marketing Date	20010701
End Marketing Date	20251231
Marketing Category Name	NDA
Application Number	NDA021110
Manufacturer	Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Substance Name	SIROLIMUS
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]