Data / Drug companies / Hydrochlorothiazide
Hydrochlorothiazide: 51 companies and 170 products in the FDA NDC directory
Hydrochlorothiazide is listed in the FDA National Drug Code Directory by 51 companies, with 170 products in commercial distribution. 165 of the products (97.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; capsule; capsule, gelatin coated, and the newest product started marketing on October 27, 2026.
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- Companies listing it
- 51
- Products
- 170
- Generic (ANDA) products
- 165 (97.1%)
- Application numbers
- 18
- Routes
- Oral
- Brand names
- Inzirqo
- openFDA record search
- api.fda.gov
Companies that list hydrochlorothiazide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 21 | tablet; capsule | Generic drugs (ANDA) | June 3, 2025 |
| Bryant Ranch Prepack | 10 | tablet; capsule | Generic drugs (ANDA) | November 1, 2019 |
| Northwind Health Company, LLC | 10 | tablet; capsule | Generic drugs (ANDA) | March 6, 2023 |
| NuCare Pharmaceuticals,Inc. | 10 | tablet | Generic drugs (ANDA) | November 1, 2019 |
| Remedyrepack Inc. | 9 | tablet; capsule | Generic drugs (ANDA) | August 26, 2026 |
| Proficient Rx LP | 7 | tablet; capsule | Generic drugs (ANDA) | June 7, 2019 |
| Preferred Pharmaceuticals Inc. | 6 | tablet; capsule | Generic drugs (ANDA) | September 24, 2026 |
| Bryant Ranch Prepack | 5 | tablet; capsule | Generic drugs (ANDA) | January 14, 2019 |
| PD-Rx Pharmaceuticals, Inc. | 5 | tablet; capsule | Generic drugs (ANDA) | September 25, 2020 |
| Proficient Rx LP | 5 | tablet; capsule, gelatin coated | Generic drugs (ANDA) | April 10, 2013 |
| QPharma, Inc. | 5 | tablet; capsule | Generic drugs (ANDA) | January 15, 2015 |
| Aphena Pharma Solutions - Tennessee, LLC | 4 | capsule; tablet | Generic drugs (ANDA) | June 7, 2019 |
| Unichem Pharmaceuticals (USA), Inc. | 4 | tablet; capsule | Generic drugs (ANDA) | April 3, 2025 |
| Accord Healthcare Inc. | 3 | tablet | Generic drugs (ANDA) | April 18, 2013 |
| American Health Packaging | 3 | tablet; capsule | Generic drugs (ANDA) | March 1, 2026 |
| Aurobindo Pharma Limited | 3 | tablet; capsule | Generic drugs (ANDA) | September 19, 2007 |
| Chartwell RX, LLC | 3 | tablet | Generic drugs (ANDA) | May 2, 2023 |
| Golden State Medical Supply, Inc. | 3 | tablet | Generic drugs (ANDA) | May 10, 2017 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 3 | tablet | Generic drugs (ANDA) | May 2, 2023 |
| Leading Pharma, LLC | 3 | tablet | Generic drugs (ANDA) | November 1, 2019 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 3 | tablet; capsule | Generic drugs (ANDA) | November 1, 2019 |
| Proficient Rx LP | 3 | tablet | Generic drugs (ANDA) | September 25, 2020 |
| ScieGen Pharmaceuticals, Inc. | 3 | tablet; capsule | Generic drugs (ANDA) | January 14, 2019 |
| St. Mary's Medical Park Pharmacy | 3 | tablet | Generic drugs (ANDA) | October 27, 2026 |
| Teva Pharmaceuticals USA, Inc. | 3 | tablet | Generic drugs (ANDA) | June 3, 2025 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet | Generic drugs (ANDA) | January 7, 1980 |
| Bryant Ranch Prepack | 2 | capsule; tablet | Generic drugs (ANDA) | January 14, 2019 |
| Direct_Rx | 2 | tablet | Generic drugs (ANDA) | September 11, 2023 |
| Exelan Pharmaceuticals Inc. | 2 | tablet | Generic drugs (ANDA) | August 30, 2016 |
| Oxford Pharmaceuticals, LLC | 2 | tablet | Generic drugs (ANDA) | September 25, 2020 |
| Redpharm Drug | 2 | tablet | Generic drugs (ANDA) | August 15, 2008 |
| Solco Healthcare US, LLC | 2 | tablet | Generic drugs (ANDA) | March 29, 2002 |
| Actavis Pharma, Inc. | 1 | capsule, gelatin coated | Authorized generics (NDA) | December 27, 1996 |
| Actavis Pharma, Inc. | 1 | tablet | Generic drugs (ANDA) | March 12, 2007 |
| Advagen Pharma Ltd | 1 | solution | Generic drugs (ANDA) | October 7, 2026 |
| Alembic Pharmaceuticals Inc. | 1 | capsule | Generic drugs (ANDA) | March 2, 2017 |
| Alembic Pharmaceuticals Limited | 1 | capsule | Generic drugs (ANDA) | March 2, 2017 |
| Ani Pharmaceuticals, Inc. | 1 | powder, for suspension | New drug applications (NDA) | January 30, 2025 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet | Generic drugs (ANDA) | May 10, 2017 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | capsule, gelatin coated | Authorized generics (NDA) | December 27, 1996 |
| AvPAK | 1 | capsule | Generic drugs (ANDA) | December 8, 2022 |
| Coupler LLC | 1 | tablet | Generic drugs (ANDA) | April 7, 2026 |
| Legacy Pharmaceutical Packaging, LLC | 1 | tablet | Generic drugs (ANDA) | January 12, 1973 |
| Northwind Health Company, LLC | 1 | tablet | Generic drugs (ANDA) | October 6, 2023 |
| NuCare Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | April 10, 2013 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | April 10, 2013 |
| Quality Care Products, LLC | 1 | tablet | Generic drugs (ANDA) | July 2, 2009 |
| Rising Pharma Holdings, Inc. | 1 | capsule | Generic drugs (ANDA) | September 19, 2007 |
| Teva Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | October 6, 2026 |
| Unit Dose Solutions, Inc. | 1 | tablet | Generic drugs (ANDA) | June 23, 2026 |
| Westminster Pharmaceuticals, LLC | 1 | capsule | Generic drugs (ANDA) | June 7, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 133 | 78.2% |
| Capsule | 31 | 18.2% |
| Capsule, gelatin coated | 4 | 2.4% |
| Powder, for suspension | 1 | 0.6% |
| Solution | 1 | 0.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 165 | 97.1% |
| Authorized generics (NDA) | 4 | 2.4% |
| New drug applications (NDA) | 1 | 0.6% |
Pharmacologic classes
| Class | Products |
|---|---|
| Thiazide Diuretic | 170 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). 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.