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"70377-012-22" National Drug Code (NDC)

Everolimus 4 BLISTER PACK in 1 CARTON (70377-012-22) / 7 TABLET in 1 BLISTER PACK
(Biocon Pharma Inc.)

NDC Code70377-012-22
Package Description4 BLISTER PACK in 1 CARTON (70377-012-22) / 7 TABLET in 1 BLISTER PACK
Product NDC70377-012
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEverolimus
Non-Proprietary NameEverolimus
Dosage FormTABLET
UsageORAL
Start Marketing Date20211001
Marketing Category NameANDA
Application NumberANDA214182
ManufacturerBiocon Pharma Inc.
Substance NameEVEROLIMUS
Strength7.5
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70377-012-22





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