Data / Drug companies / Partial Cholinergic Nicotinic Agonist
Partial Cholinergic Nicotinic Agonist drugs: 2 drugs from 31 companies in the FDA NDC directory
Partial Cholinergic Nicotinic Agonist is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 64 products in this class from 31 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on April 29, 2026.
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- 31Companies
- 64Products
- 2Drugs by generic name
Drugs in the Partial Cholinergic Nicotinic Agonist class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Varenicline tartrate | 40 | 23 |
| Varenicline | 24 | 11 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 8 | tablet, film coated | Generic drugs (ANDA) | December 10, 2024 |
| Apotex Corp. | 4 | tablet, film coated | Generic drugs (ANDA) | January 30, 2023 |
| Ajanta Pharma USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 31, 2024 |
| Ascend Laboratories, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | August 25, 2023 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | May 2, 2025 |
| AvKARE | 2 | tablet, film coated | Generic drugs (ANDA) | September 14, 2023 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | January 30, 2023 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | October 23, 2023 |
| Dr. Reddy's Laboratories Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | December 13, 2024 |
| Florida Pharmaceutical Products, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 1, 2024 |
| Glenmark Pharmaceuticals Inc., USA | 2 | tablet, film coated | Generic drugs (ANDA) | August 22, 2023 |
| Indoco Remedies Limited | 2 | tablet, film coated | Generic drugs (ANDA) | November 1, 2024 |
| Kanchan Healthcare Inc | 2 | tablet, film coated | Generic drugs (ANDA) | October 1, 2023 |
| Leading Pharma, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | October 1, 2023 |
| Lupin Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 9, 2024 |
| Macleods Pharmaceuticals Limited | 2 | tablet, film coated | Generic drugs (ANDA) | December 10, 2024 |
| Major Pharmaceuticals | 2 | tablet, film coated | Generic drugs (ANDA) | December 18, 2023 |
| Marlex Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 1, 2025 |
| Micro Labs Limited | 2 | tablet, film coated | Generic drugs (ANDA) | December 1, 2025 |
| NorthStar RxLLC | 2 | tablet, film coated | Generic drugs (ANDA) | September 23, 2024 |
| Par Health USA, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | September 21, 2021 |
| Pfizer Laboratories Div Pfizer Inc | 2 | tablet, film coated | New drug applications (NDA) | May 10, 2006 |
| Umedica Laboratories USA Inc. | 2 | tablet | Generic drugs (ANDA) | January 9, 2026 |
| Zydus Lifesciences Limited | 2 | tablet, film coated | Generic drugs (ANDA) | June 13, 2023 |
| Zydus Pharmaceuticals USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 13, 2023 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | December 9, 2025 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | New drug applications (NDA) | May 10, 2006 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | January 30, 2023 |
| Harrow Eye, LLC | 1 | spray | New drug applications (NDA) | October 20, 2021 |
| Proficient Rx LP | 1 | tablet, film coated | New drug applications (NDA) | May 10, 2006 |
| Remedyrepack Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 29, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 61 | 95.3% |
| Tablet | 2 | 3.1% |
| Spray | 1 | 1.6% |
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.