"0078-0669-13" National Drug Code (NDC)

Arzerra 3 VIAL, SINGLE-USE in 1 CARTON (0078-0669-13) / 5 mL in 1 VIAL, SINGLE-USE (0078-0669-61)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0669-13
Package Description3 VIAL, SINGLE-USE in 1 CARTON (0078-0669-13) / 5 mL in 1 VIAL, SINGLE-USE (0078-0669-61)
Product NDC0078-0669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameArzerra
Non-Proprietary NameOfatumumab
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS
Start Marketing Date20160201
Marketing Category NameBLA
Application NumberBLA125326
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameOFATUMUMAB
Strength20
Strength Unitmg/mL
Pharmacy ClassesCD20-directed Antibody Interactions [MoA], CD20-directed Cytolytic Antibody [EPC]

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