"51991-822-28" National Drug Code (NDC)

NDC Code	51991-822-28
Package Description	4 BLISTER PACK in 1 CARTON (51991-822-28) / 7 TABLET in 1 BLISTER PACK (51991-822-99)
Product NDC	51991-822
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Everolimus
Non-Proprietary Name	Everolimus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210305
Marketing Category Name	ANDA
Application Number	ANDA205426
Manufacturer	Breckenridge Pharmaceutical, Inc.
Substance Name	EVEROLIMUS
Strength	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]