"0007-4641-13" National Drug Code (NDC)

Promacta 30 TABLET, FILM COATED in 1 BOTTLE (0007-4641-13)
(GlaxoSmithKline LLC)

NDC Code0007-4641-13
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0007-4641-13)
Product NDC0007-4641
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePromacta
Non-Proprietary NameEltrombopag Olamine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20081124
End Marketing Date20190430
Marketing Category NameNDA
Application NumberNDA022291
ManufacturerGlaxoSmithKline LLC
Substance NameELTROMBOPAG OLAMINE
Strength50
Strength Unitmg/1
Pharmacy ClassesIncreased Megakaryocyte Maturation [PE],Increased Platelet Production [PE],Thrombopoietin Receptor Agonist [EPC],Thrombopoietin Receptor Agonists [MoA],Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA],Breast Cancer Resistance Protein Inhibitors [MoA],UGT1A1 Inhibitors [MoA],UGT1A3 Inhibitors [MoA],UGT1A4 Inhibitors [MoA],UGT1A6 Inhibitors [MoA],UGT1A9 Inhibitors [MoA],UGT2B7 Inhibitors [MoA],UGT2B15 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0007-4641-13