PROMACTA - 0007-4641-13 - (eltrombopag olamine)

Alphabetical Index


Drug Information of PROMACTA

Product NDC: 0007-4641
Proprietary Name: PROMACTA
Non Proprietary Name: eltrombopag olamine
Active Ingredient(s): 50    mg/1 & nbsp;   eltrombopag olamine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of PROMACTA

Product NDC: 0007-4641
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022291
Marketing Category: NDA
Start Marketing Date: 20081124

Package Information of PROMACTA

Package NDC: 0007-4641-13
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0007-4641-13)

NDC Information of PROMACTA

NDC Code 0007-4641-13
Proprietary Name PROMACTA
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0007-4641-13)
Product NDC 0007-4641
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name eltrombopag olamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081124
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ELTROMBOPAG OLAMINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Increased Megakaryocyte Maturation [PE],Increased Platelet Production [PE],Thrombopoiesis Stimulating Agent [EPC],Thrombopoietin Receptor Agonists [MoA],Thrombopoietin Receptor Interactions [MoA]

Complete Information of PROMACTA


General Information