"50242-082-02" National Drug Code (NDC)

Lucentis 1 VIAL, SINGLE-USE in 1 CARTON (50242-082-02) > .05 mL in 1 VIAL, SINGLE-USE
(Genentech, Inc.)

NDC Code50242-082-02
Package Description1 VIAL, SINGLE-USE in 1 CARTON (50242-082-02) > .05 mL in 1 VIAL, SINGLE-USE
Product NDC50242-082
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLucentis
Non-Proprietary NameRanibizumab
Dosage FormINJECTION, SOLUTION
UsageINTRAVITREAL
Start Marketing Date20120810
Marketing Category NameBLA
Application NumberBLA125156
ManufacturerGenentech, Inc.
Substance NameRANIBIZUMAB
Strength6
Strength Unitmg/mL
Pharmacy ClassesVascular Endothelial Growth Factor Inhibitor [EPC], Vascular Endothelial Growth Factor Inhibitors [MoA]

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