"25682-022-01" National Drug Code (NDC)

Ultomiris 1 VIAL, GLASS in 1 CARTON (25682-022-01) / 30 mL in 1 VIAL, GLASS
(Alexion Pharmaceuticals Inc.)

NDC Code25682-022-01
Package Description1 VIAL, GLASS in 1 CARTON (25682-022-01) / 30 mL in 1 VIAL, GLASS
Product NDC25682-022
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameUltomiris
Non-Proprietary NameRavulizumab
Dosage FormSOLUTION, CONCENTRATE
UsageINTRAVENOUS
Start Marketing Date20181221
Marketing Category NameBLA
Application NumberBLA761108
ManufacturerAlexion Pharmaceuticals Inc.
Substance NameRAVULIZUMAB
Strength300
Strength Unitmg/30mL
Pharmacy ClassesComplement Inhibitor [EPC], Complement Inhibitors [MoA]

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