"0024-5840-01" National Drug Code (NDC)

Zaltrap 1 VIAL in 1 CARTON (0024-5840-01) / 4 mL in 1 VIAL
(sanofi-aventis U.S. LLC)

NDC Code0024-5840-01
Package Description1 VIAL in 1 CARTON (0024-5840-01) / 4 mL in 1 VIAL
Product NDC0024-5840
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZaltrap
Non-Proprietary NameZiv-aflibercept
Dosage FormSOLUTION, CONCENTRATE
UsageINTRAVENOUS
Start Marketing Date20120803
Marketing Category NameBLA
Application NumberBLA125418
Manufacturersanofi-aventis U.S. LLC
Substance NameAFLIBERCEPT
Strength100
Strength Unitmg/4mL
Pharmacy ClassesVascular Endothelial Growth Factor Inhibitor [EPC], Vascular Endothelial Growth Factor Inhibitors [MoA]

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