Active ingredient
Lusutrombopag
3 finished FDA listings contain Lusutrombopag as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- LUSUTROMBOPAG
- Dosage forms
- Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 3
- Strengths listed
- 3 mg/1
- Brand names in FDA listings
- Mulpleta
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 2054984
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| NDA 210923 | VANCOCIN ITALIA | 2018-07-31 | 3 |
Official labeling on DailyMed
- MULPLETA (LUSUTROMBOPAG) TABLET, FILM COATED [VANCOCIN ITALIA SRL] · version 6 · 2025-12-10
- MULPLETA (LUSUTROMBOPAG) TABLET, FILM COATED [EDDINGPHARM (U. S. ) INC.] · version 3 · 2025-12-04
- MULPLETA (LUSUTROMBOPAG) TABLET, FILM COATED [SHIONOGI INC.] · version 7 · 2020-11-02
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.