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"50242-135-01" National Drug Code (NDC)

Actemra 1 VIAL, SINGLE-USE in 1 BOX (50242-135-01) / 4 mL in 1 VIAL, SINGLE-USE
(Genentech, Inc.)

NDC Code50242-135-01
Package Description1 VIAL, SINGLE-USE in 1 BOX (50242-135-01) / 4 mL in 1 VIAL, SINGLE-USE
Product NDC50242-135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameActemra
Non-Proprietary NameTocilizumab
Dosage FormINJECTION, SOLUTION, CONCENTRATE
UsageINTRAVENOUS
Start Marketing Date20100108
Marketing Category NameBLA
Application NumberBLA125276
ManufacturerGenentech, Inc.
Substance NameTOCILIZUMAB
Strength80
Strength Unitmg/4mL
Pharmacy ClassesInterleukin 6 Receptor Antagonists [MoA], Interleukin-6 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50242-135-01





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