"49884-119-91" National Drug Code (NDC)

NDC Code	49884-119-91
Package Description	28 BLISTER PACK in 1 CARTON (49884-119-91) / 1 TABLET in 1 BLISTER PACK (49884-119-52)
Product NDC	49884-119
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20191210
Marketing Category Name	ANDA
Application Number	ANDA207934
Manufacturer	ENDO USA, Inc.
Substance Name	EVEROLIMUS
Strength	2.5
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]