Active ingredient
Nefazodone
6 finished FDA listings contain Nefazodone as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- NEFAZODONE HYDROCHLORIDE
- Dosage forms
- Tablet
- Routes
- Oral
- Manufacturers / labelers
- 2
- Strengths listed
- 100 mg/1 · 150 mg/1 · 200 mg/1 · 250 mg/1 · 50 mg/1
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 31565
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 |
|---|---|---|---|
| ANDA 076037 | TEVA | 2003-09-16 | 6 |
Official labeling on DailyMed
- NEFAZODONE HYDROCHLORIDE TABLET [TEVA PHARMACEUTICALS USA, INC.] · version 12 · 2025-11-17
- NEFAZODONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] · version 19 · 2025-09-08
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.