Active ingredient
Fezolinetant
3 finished FDA listings contain Fezolinetant as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- FEZOLINETANT
- Dosage forms
- Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 1
- Strengths listed
- 45 mg/1
- Brand names in FDA listings
- Veozah
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 2637134
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 216578 | ASTELLAS | 2023-05-12 | 3 |
Official labeling on DailyMed
- VEOZAH (FEZOLINETANT) TABLET, FILM COATED [ASTELLAS PHARMA US, INC.] · version 8 · 2026-03-06
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.