"70954-774-20" National Drug Code (NDC)

NDC Code	70954-774-20
Package Description	28 BLISTER PACK in 1 CARTON (70954-774-20) / 1 TABLET, FOR SUSPENSION in 1 BLISTER PACK (70954-774-10)
Product NDC	70954-774
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET, FOR SUSPENSION
Usage	ORAL
Start Marketing Date	20251010
Marketing Category Name	ANDA
Application Number	ANDA220597
Manufacturer	ANI Pharmaceuticals, Inc.
Substance Name	EVEROLIMUS
Strength	3
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]