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PROMACTA

NDC 0078-0685 · Novartis Pharmaceuticals Corporation

Generic nameeltrombopag olamine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ELTROMBOPAG OLAMINE
Strength25 mg/1
Pharmacologic classBreast Cancer Resistance Protein Inhibitors [MoA], Increased Megakaryocyte Maturation [PE], Increased Platelet Production [PE], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Thrombopoietin Receptor Agonist [EPC], Thrombopoietin Receptor Agonists [MoA], UGT1A1 Inhibitors [MoA], UGT1A3 Inhibitors [MoA], UGT1A4 Inhibitors [MoA], UGT1A6 Inhibitors [MoA], UGT1A9 Inhibitors [MoA], UGT2B15 Inhibitors [MoA], UGT2B7 Inhibitors [MoA]
Marketing categoryNDA

Packages

0078-0685-15 — 30 TABLET, FILM COATED in 1 BOTTLE (0078-0685-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0962 — Eltrombopag Olamine, 0054-0963 — Eltrombopag Olamine, 0054-0964 — Eltrombopag Olamine, 0054-0965 — Eltrombopag Olamine, 0078-0684 — eltrombopag olamine, 0078-0686 — eltrombopag olamine, 0078-0687 — eltrombopag olamine, 0078-0697 — eltrombopag olamine, 0078-0972 — eltrombopag olamine, 31722-300 — Eltrombopag olamine, 31722-301 — Eltrombopag olamine, 31722-841 — ELTROMBOPAG, 31722-842 — ELTROMBOPAG, 31722-843 — ELTROMBOPAG, 31722-844 — ELTROMBOPAG, 42291-932 — Eltrombopag, 42291-933 — Eltrombopag, 42291-934 — Eltrombopag, 42291-935 — Eltrombopag, 43598-151 — eltrombopag, +35 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.