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"50242-922-01" National Drug Code (NDC)
Hemlibra 1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE
(Genentech, Inc.)
NDC Code
50242-922-01
Package Description
1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE
Product NDC
50242-922
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hemlibra
Non-Proprietary Name
Emicizumab
Dosage Form
INJECTION, SOLUTION
Usage
SUBCUTANEOUS
Start Marketing Date
20171116
Marketing Category Name
BLA
Application Number
BLA761083
Manufacturer
Genentech, Inc.
Substance Name
EMICIZUMAB
Strength
105
Strength Unit
mg/.7mL
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50242-922-01