Active ingredient
Flunisolide
3 finished FDA listings contain Flunisolide as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- FLUNISOLIDE, FLUNISOLIDE ANHYDROUS
- Dosage forms
- Solution
- Routes
- Nasal
- Manufacturers / labelers
- 3
- Strengths listed
- .25 mg/ml
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 25120
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 074805 | BAUSCH | 2002-02-20 | 2 |
| ANDA 207802 | RICONPHARMA LLC | 2022-06-16 | 1 |
Official labeling on DailyMed
- FLUNISOLIDE SOLUTION [BAUSCH & LOMB INCORPORATED] · version 19 · 2025-11-17
- FLUNISOLIDE SOLUTION [OCEANSIDE PHARMACEUTICALS] · version 7 · 2025-08-04
- FLUNISOLIDE SOLUTION [INGENUS PHARMACEUTICALS, LLC] · version 2 · 2025-05-05
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.