"72603-256-01" National Drug Code (NDC)

NDC Code	72603-256-01
Package Description	30 TABLET in 1 BOTTLE (72603-256-01)
Product NDC	72603-256
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20241001
Marketing Category Name	ANDA
Application Number	ANDA214182
Manufacturer	NorthStar RxLLC
Substance Name	EVEROLIMUS
Strength	7.5
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]