Data / Drug companies / Colchicine
Colchicine: 34 companies and 53 products in the FDA NDC directory
Colchicine is listed in the FDA National Drug Code Directory by 34 companies, with 53 products in commercial distribution. 42 of the products (79.2%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated; capsule, and the newest product started marketing on August 27, 2026.
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- Companies listing it
- 34
- Products
- 53
- Generic (ANDA) products
- 42 (79.2%)
- Application numbers
- 19
- Routes
- Oral
- Brand names
- Colcrys, Gloperba
- openFDA record search
- api.fda.gov
Companies that list colchicine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 4 | tablet, film coated; capsule | Generic drugs (ANDA) | April 29, 2024 |
| Bryant Ranch Prepack | 4 | tablet, film coated; tablet | Authorized generics (NDA) | February 10, 2019 |
| A-S Medication Solutions | 3 | tablet; capsule | Generic drugs (ANDA) | November 10, 2020 |
| Direct_Rx | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | August 27, 2026 |
| American Health Packaging | 2 | capsule; tablet, film coated | New drug applications (NDA) | August 1, 2023 |
| Aurobindo Pharma Limited | 2 | tablet; capsule | Generic drugs (ANDA) | April 29, 2024 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated; capsule | Generic drugs (ANDA) | April 29, 2024 |
| Coupler LLC | 2 | capsule | New drug applications (NDA) | December 30, 2025 |
| Granules Pharmaceuticals Inc. | 2 | tablet, film coated; capsule | Generic drugs (ANDA) | April 29, 2024 |
| Major Pharmaceuticals | 2 | tablet, film coated; capsule | Generic drugs (ANDA) | May 13, 2020 |
| Remedyrepack Inc. | 2 | tablet, film coated; tablet | Generic drugs (ANDA) | January 29, 2024 |
| Zydus Lifesciences Limited | 2 | tablet | Generic drugs (ANDA) | May 10, 2021 |
| Zydus Pharmaceuticals USA Inc. | 2 | tablet | Generic drugs (ANDA) | May 10, 2021 |
| Amneal Pharmaceuticals LLC | 1 | tablet | Generic drugs (ANDA) | September 30, 2016 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | February 5, 2020 |
| Ascend Laboratories, LLC | 1 | tablet | Generic drugs (ANDA) | February 10, 2019 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | September 15, 2021 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | February 10, 2019 |
| Chartwell RX, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | March 26, 2023 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet | Generic drugs (ANDA) | June 11, 2020 |
| Golden State Medical Supply, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | February 5, 2020 |
| Hikma Pharmaceuticals USA Inc. | 1 | capsule | Authorized generics (NDA) | October 1, 2014 |
| Macleods Pharmaceuticals Limited | 1 | tablet | Generic drugs (ANDA) | April 24, 2017 |
| Micro Labs Limited | 1 | capsule | Generic drugs (ANDA) | February 18, 2026 |
| Mylan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | November 25, 2019 |
| NorthStar Rx LLC | 1 | tablet | Generic drugs (ANDA) | November 10, 2020 |
| NuCare Pharmaceuticals,Inc. | 1 | tablet | Generic drugs (ANDA) | February 10, 2019 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 13, 2021 |
| Par Health USA, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 27, 2022 |
| Par Health USA, LLC | 1 | capsule | Generic drugs (ANDA) | November 1, 2023 |
| Proficient Rx LP | 1 | tablet, film coated | New drug applications (NDA) | September 1, 2009 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | June 11, 2020 |
| Scilex Pharmaceuticals Inc. | 1 | solution | New drug applications (NDA) | January 31, 2024 |
| St. Mary's Medical Park Pharmacy | 1 | tablet | Generic drugs (ANDA) | April 23, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 22 | 41.5% |
| Tablet, film coated | 18 | 34% |
| Capsule | 12 | 22.6% |
| Solution | 1 | 1.9% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 42 | 79.2% |
| New drug applications (NDA) | 7 | 13.2% |
| Authorized generics (NDA) | 4 | 7.5% |
Pharmacologic classes
| Class | Products |
|---|---|
| Alkaloid | 45 |
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.