Data / Drug companies / Olopatadine hydrochloride ophthalmic solution
Olopatadine hydrochloride ophthalmic solution: 8 companies and 8 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Olopatadine hydrochloride ophthalmic solution is listed in the FDA National Drug Code Directory by 8 companies, with 8 products in commercial distribution. 8 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are solution; solution/ drops, and the newest product started marketing on December 22, 2025.
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- Companies listing it
- 8
- Products
- 8
- Generic (ANDA) products
- 8 (100.0%)
- Application numbers
- 4
- Routes
- Ophthalmic
- Brand names
- Once Daily Relief, Olopatadine Hydrochloride
- openFDA record search
- api.fda.gov
Companies that list olopatadine hydrochloride ophthalmic solution
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bausch & Lomb Incorporated | 1 | solution | Generic drugs (ANDA) | December 2, 2024 |
| Cardinal Health 110, LLC. DBA Leader | 1 | solution | Generic drugs (ANDA) | April 15, 2025 |
| H E B | 1 | solution | Generic drugs (ANDA) | March 7, 2022 |
| Rugby Laboratories | 1 | solution/ drops | Generic drugs (ANDA) | April 15, 2025 |
| Target Corporation | 1 | solution | Generic drugs (ANDA) | April 15, 2025 |
| Target Corporation | 1 | solution/ drops | Generic drugs (ANDA) | October 22, 2021 |
| Walgreen Company | 1 | solution | Generic drugs (ANDA) | December 22, 2025 |
| Walmart Inc. | 1 | solution | Generic drugs (ANDA) | April 15, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution | 6 | 75% |
| Solution/ drops | 2 | 25% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 8 | 100% |
Pharmacologic classes
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.