NDC 0480-4015 – Eltrombopag

Eltrombopag Olamine 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0480-4015

Product details

Brand name
Eltrombopag
Generic name
Eltrombopag
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209938
Marketed since
September 17, 2026
Listing expires
December 31, 2027
Pharmacologic class
Thrombopoietin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Eltrombopag →

Package NDC codes (1)

Package NDCDescriptionSince
0480-4015-5630 TABLET, FILM COATED in 1 BOTTLE (0480-4015-56)Sep 17, 2026

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