Active ingredient
Dacomitinib
3 finished FDA listings contain Dacomitinib as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- DACOMITINIB
- Dosage forms
- Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 1
- Strengths listed
- 15 mg/1 · 30 mg/1 · 45 mg/1
- Brand names in FDA listings
- Vizimpro
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 2058849
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 211288 | PFIZER | 2018-09-27 | 3 |
Official labeling on DailyMed
- VIZIMPRO (DACOMITINIB) TABLET, FILM COATED [PFIZER LABORATORIES DIV PFIZER INC] · version 9 · 2026-06-25
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.