"0078-0686-55" National Drug Code (NDC)

Promacta 14 TABLET, FILM COATED in 1 BOTTLE (0078-0686-55)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0686-55
Package Description14 TABLET, FILM COATED in 1 BOTTLE (0078-0686-55)
Product NDC0078-0686
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePromacta
Non-Proprietary NameEltrombopag Olamine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160407
Marketing Category NameNDA
Application NumberNDA022291
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameELTROMBOPAG OLAMINE
Strength50
Strength Unitmg/1
Pharmacy ClassesBreast Cancer Resistance Protein Inhibitors [MoA], Increased Megakaryocyte Maturation [PE], Increased Platelet Production [PE], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Thrombopoietin Receptor Agonist [EPC], Thrombopoietin Receptor Agonists [MoA], UGT1A1 Inhibitors [MoA], UGT1A3 Inhibitors [MoA], UGT1A4 Inhibitors [MoA], UGT1A6 Inhibitors [MoA], UGT1A9 Inhibitors [MoA], UGT2B15 Inhibitors [MoA], UGT2B7 Inhibitors [MoA]

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