PROMACTA

Product NDC

0007-4642

11-digit product format

000074642

Labeler code

0007

Product ID

0007-4642_c7c46a73-1f77-45f6-ab60-1aa8f9e87463

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

eltrombopag olamine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

GlaxoSmithKline LLC

Application

NDA022291

Marketing category

NDA

Marketing start

2009-01-05

Marketing end

2019-03-31

Substance

ELTROMBOPAG OLA

Active strength

75 mg/1

Pharmacologic classes

Increased Megak

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record