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"0173-0821-01" National Drug Code (NDC)

Arzerra 1 VIAL in 1 CARTON (0173-0821-01) > 50 mL in 1 VIAL
(GlaxoSmithKline LLC)

NDC Code0173-0821-01
Package Description1 VIAL in 1 CARTON (0173-0821-01) > 50 mL in 1 VIAL
Product NDC0173-0821
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameArzerra
Non-Proprietary NameOfatumumab
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS
Start Marketing Date20110722
End Marketing Date20170831
Marketing Category NameBLA
Application NumberBLA125326
ManufacturerGlaxoSmithKline LLC
Substance NameOFATUMUMAB
Strength20
Strength Unitmg/mL
Pharmacy ClassesCD20-directed Cytolytic Antibody [EPC],CD20-directed Antibody Interactions [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0821-01





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