"81864-103-30" National Drug Code (NDC)

Ojjaara 30 TABLET in 1 BOTTLE (81864-103-30)
(GlaxoSmithKline LLC)

NDC Code81864-103-30
Package Description30 TABLET in 1 BOTTLE (81864-103-30)
Product NDC81864-103
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOjjaara
Non-Proprietary NameMomelotinib
Dosage FormTABLET
UsageORAL
Start Marketing Date20230915
Marketing Category NameNDA
Application NumberNDA216873
ManufacturerGlaxoSmithKline LLC
Substance NameMOMELOTINIB DIHYDROCHLORIDE MONOHYDRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesBreast Cancer Resistance Protein Inhibitors [MoA], Kinase Inhibitor [EPC], Kinase Inhibitors [MoA]

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