"0007-4641-61" National Drug Code (NDC)

NDC Code	0007-4641-61
Package Description	14 TABLET, FILM COATED in 1 BOTTLE (0007-4641-61)
Product NDC	0007-4641
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Promacta
Non-Proprietary Name	Eltrombopag Olamine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20081124
End Marketing Date	20190430
Marketing Category Name	NDA
Application Number	NDA022291
Manufacturer	GlaxoSmithKline LLC
Substance Name	ELTROMBOPAG OLAMINE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Increased 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]