NDC 0007-4642

PROMACTA

Eltrombopag Olamine

PROMACTA is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Glaxosmithkline Llc. The primary component is Eltrombopag Ola.

• Product ID: 0007-4642_c7c46a73-1f77-45f6-ab60-1aa8f9e87463
• NDC: 0007-4642
• Product Type: Human Prescription Drug
• Proprietary Name: PROMACTA
• Generic Name: Eltrombopag Olamine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2009-01-05
• Marketing End Date: 2019-03-31
• Marketing Category: NDA /
• Application Number: NDA022291
• Labeler Name: GlaxoSmithKline LLC
• Substance Name: ELTROMBOPAG OLA
• Active Ingredient Strength: 75 mg/1
• Pharm Classes: Increased Megak
• NDC Exclude Flag: N

Packaging

NDC SPL Data Element Entries

NDC 0007-4642-13 [00007464213]

PROMACTA TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA022291
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-01-05
• Marketing End Date: 2019-03-31

Drug Details

NDC Crossover Matching brand name "PROMACTA" or generic name "Eltrombopag Olamine"

NDC	Brand Name	Generic Name
0007-4640	PROMACTA	eltrombopag olamine
0007-4641	PROMACTA	eltrombopag olamine
0007-4642	PROMACTA	eltrombopag olamine
0007-4643	PROMACTA	eltrombopag olamine
0078-0684	PROMACTA	eltrombopag olamine
0078-0685	PROMACTA	eltrombopag olamine
0078-0686	PROMACTA	eltrombopag olamine
0078-0687	PROMACTA	eltrombopag olamine
0078-0697	PROMACTA	eltrombopag olamine
0078-0972	PROMACTA	PROMACTA