Data / Drug companies / Haloperidol
Haloperidol: 32 companies and 165 products in the FDA NDC directory
Haloperidol is listed in the FDA National Drug Code Directory by 32 companies, with 165 products in commercial distribution. 165 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; solution; solution, concentrate, and the newest product started marketing on September 14, 2026.
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- Companies listing it
- 32
- Products
- 165
- Generic (ANDA) products
- 165 (100.0%)
- Application numbers
- 14
- Routes
- Oral, Intramuscular
- openFDA record search
- api.fda.gov
Companies that list haloperidol
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 12 | tablet | Generic drugs (ANDA) | January 5, 2026 |
| Method Pharmaceuticals, LLC | 12 | tablet | Generic drugs (ANDA) | June 5, 2025 |
| Remedyrepack Inc. | 11 | tablet | Generic drugs (ANDA) | August 12, 2026 |
| Coupler LLC | 10 | tablet | Generic drugs (ANDA) | August 3, 2026 |
| Bryant Ranch Prepack | 7 | tablet | Generic drugs (ANDA) | November 25, 2019 |
| Bryant Ranch Prepack | 7 | tablet | Generic drugs (ANDA) | April 19, 2024 |
| AiPing Pharmaceutical, Inc. | 6 | tablet | Generic drugs (ANDA) | April 8, 2026 |
| Ajanta Pharma USA Inc. | 6 | tablet | Generic drugs (ANDA) | September 14, 2026 |
| Amici Pharma, Inc. | 6 | tablet | Generic drugs (ANDA) | April 18, 2022 |
| Aurobindo Pharma Limited | 6 | tablet | Generic drugs (ANDA) | April 19, 2024 |
| Creekwood Pharmaceuticals LLC | 6 | tablet | Generic drugs (ANDA) | January 5, 2026 |
| Innogenix, Inc. | 6 | tablet | Generic drugs (ANDA) | February 18, 2021 |
| Lifestar Pharma LLC | 6 | tablet | Generic drugs (ANDA) | April 11, 2024 |
| Marlex Pharmaceuticals, Inc. | 6 | tablet | Generic drugs (ANDA) | August 1, 2022 |
| Novadoz Pharmaceuticals LLC | 6 | tablet | Generic drugs (ANDA) | November 18, 2022 |
| PD-Rx Pharmaceuticals, Inc. | 6 | tablet | Generic drugs (ANDA) | April 8, 2026 |
| Upsher-Smith Laboratories, LLC | 6 | tablet | Generic drugs (ANDA) | January 9, 2020 |
| Zydus Lifesciences Limited | 6 | tablet | Generic drugs (ANDA) | February 1, 2023 |
| Zydus Pharmaceuticals USA Inc. | 6 | tablet | Generic drugs (ANDA) | February 1, 2023 |
| Major Pharmaceuticals | 4 | tablet | Generic drugs (ANDA) | January 28, 2025 |
| Mylan Institutional Inc. | 4 | tablet | Generic drugs (ANDA) | February 15, 2004 |
| Mylan Pharmaceuticals Inc. | 4 | tablet | Generic drugs (ANDA) | June 10, 1986 |
| Safecor Health, LLC | 3 | tablet | Generic drugs (ANDA) | June 1, 2026 |
| American Health Packaging | 2 | tablet | Generic drugs (ANDA) | April 4, 2008 |
| American Health Packaging | 2 | tablet; solution | Generic drugs (ANDA) | April 15, 2024 |
| Cardinal Health 107, LLC | 2 | tablet | Generic drugs (ANDA) | January 3, 2008 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 2 | tablet | Generic drugs (ANDA) | April 11, 2024 |
| Advagen Pharma Ltd | 1 | solution, concentrate | Generic drugs (ANDA) | January 31, 2024 |
| Henry Schein, Inc. | 1 | injection, solution | Generic drugs (ANDA) | January 11, 2022 |
| Lannett Company, Inc. | 1 | solution | Generic drugs (ANDA) | September 28, 1993 |
| Pai Holdings, LLC DBA Pai Pharma | 1 | solution | Generic drugs (ANDA) | November 10, 2009 |
| Unit Dose Solutions, Inc. | 1 | tablet | Generic drugs (ANDA) | June 23, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 160 | 97% |
| Solution | 3 | 1.8% |
| Solution, concentrate | 1 | 0.6% |
| Injection, solution | 1 | 0.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 165 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Typical Antipsychotic | 165 |
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.