Active ingredient
Brinzolamide
6 finished FDA listings contain Brinzolamide as their only active ingredient; 1 combination products also contain it.
FDA NDC Directory
- Ingredient names as written by FDA
- BRINZOLAMIDE
- Dosage forms
- Suspension/ Drops
- Routes
- Ophthalmic
- Manufacturers / labelers
- 5
- Strengths listed
- 10 mg/ml
- Brand names in FDA listings
- Azopt
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 194881
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 020816 | SANDOZ | 1998-04-01 | 2 |
| ANDA 204884 | BAUSCH AND LOMB | 2021-08-18 | 2 |
| ANDA 211914 | PADAGIS US | 2023-07-28 | 2 |
Official labeling on DailyMed
- BRINZOLAMIDE SUSPENSION/ DROPS [OCEANSIDE PHARMACEUTICALS.] · version 2 · 2026-04-22
- BRINZOLAMIDE SUSPENSION/ DROPS [SANDOZ INC] · version 4 · 2025-11-24
- BRINZOLAMIDE SUSPENSION/ DROPS [PADAGIS US LLC] · version 4 · 2025-09-10
- AZOPT (BRINZOLAMIDE) SUSPENSION/ DROPS [SANDOZ INC] · version 1 · 2024-10-25
- BRINZOLAMIDE SUSPENSION/ DROPS [BRYANT RANCH PREPACK] · version 100 · 2023-12-25
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.