"70377-012-23" National Drug Code (NDC)

NDC Code	70377-012-23
Package Description	4 BLISTER PACK in 1 CARTON (70377-012-23) / 7 TABLET in 1 BLISTER PACK
Product NDC	70377-012
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20211001
Marketing Category Name	ANDA
Application Number	ANDA214182
Manufacturer	Biocon Pharma Inc.
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]