"72319-016-60" National Drug Code (NDC)

NDC Code	72319-016-60
Package Description	60 BLISTER PACK in 1 CARTON (72319-016-60) / 10 TABLET in 1 BLISTER PACK (72319-016-10)
Product NDC	72319-016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20260807
Marketing Category Name	ANDA
Application Number	ANDA219464
Manufacturer	i3 Pharmaceuticals, LLC
Substance Name	EVEROLIMUS
Strength	.75
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]