"0093-7769-24" National Drug Code (NDC)

Everolimus 28 BLISTER PACK in 1 CARTON (0093-7769-24) / 1 TABLET in 1 BLISTER PACK (0093-7769-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7769-24
Package Description28 BLISTER PACK in 1 CARTON (0093-7769-24) / 1 TABLET in 1 BLISTER PACK (0093-7769-19)
Product NDC0093-7769
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEverolimus
Non-Proprietary NameEverolimus
Dosage FormTABLET
UsageORAL
Start Marketing Date20231023
Marketing Category NameANDA
Application NumberANDA210050
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameEVEROLIMUS
Strength10
Strength Unitmg/1
Pharmacy ClassesCytochrome 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]

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