"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 Code50242-922-01
Package Description1 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USE
Product NDC50242-922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHemlibra
Non-Proprietary NameEmicizumab
Dosage FormINJECTION, SOLUTION
UsageSUBCUTANEOUS
Start Marketing Date20171116
Marketing Category NameBLA
Application NumberBLA761083
ManufacturerGenentech, Inc.
Substance NameEMICIZUMAB
Strength105
Strength Unitmg/.7mL

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