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"50242-136-01" National Drug Code (NDC)
Actemra 1 VIAL, SINGLE-USE in 1 BOX (50242-136-01) / 10 mL in 1 VIAL, SINGLE-USE
(Genentech, Inc.)
NDC Code
50242-136-01
Package Description
1 VIAL, SINGLE-USE in 1 BOX (50242-136-01) / 10 mL in 1 VIAL, SINGLE-USE
Product NDC
50242-136
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Actemra
Non-Proprietary Name
Tocilizumab
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Usage
INTRAVENOUS
Start Marketing Date
20100108
Marketing Category Name
BLA
Application Number
BLA125276
Manufacturer
Genentech, Inc.
Substance Name
TOCILIZUMAB
Strength
200
Strength Unit
mg/10mL
Pharmacy Classes
Interleukin 6 Receptor Antagonists [MoA], Interleukin-6 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50242-136-01