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"25682-025-01" National Drug Code (NDC)

Ultomiris 1 VIAL, GLASS in 1 CARTON (25682-025-01) / 3 mL in 1 VIAL, GLASS
(Alexion Pharmaceuticals Inc.)

NDC Code25682-025-01
Package Description1 VIAL, GLASS in 1 CARTON (25682-025-01) / 3 mL in 1 VIAL, GLASS
Product NDC25682-025
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameUltomiris
Non-Proprietary NameRavulizumab
Dosage FormSOLUTION, CONCENTRATE
UsageINTRAVENOUS
Start Marketing Date20201009
Marketing Category NameBLA
Application NumberBLA761108
ManufacturerAlexion Pharmaceuticals Inc.
Substance NameRAVULIZUMAB
Strength300
Strength Unitmg/3mL
Pharmacy ClassesComplement Inhibitor [EPC], Complement Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/25682-025-01





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