Data / Drug companies / Diclofenac potassium
Diclofenac potassium: 42 companies and 56 products in the FDA NDC directory
Diclofenac potassium is listed in the FDA National Drug Code Directory by 42 companies, with 56 products in commercial distribution. 50 of the products (89.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; capsule, liquid filled; tablet, coated, and the newest product started marketing on September 18, 2026.
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- Companies listing it
- 42
- Products
- 56
- Generic (ANDA) products
- 50 (89.3%)
- Application numbers
- 17
- Routes
- Oral
- Brand names
- Zipsor, Lofena, Cambia
- openFDA record search
- api.fda.gov
Companies that list diclofenac potassium
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Advagen Pharma Ltd | 3 | tablet, coated | Generic drugs (ANDA) | September 18, 2026 |
| Bryant Ranch Prepack | 3 | tablet, film coated; tablet, coated | Generic drugs (ANDA) | March 24, 2022 |
| Advanced Rx of Tennessee, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | December 15, 2024 |
| Amici Pharma, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 18, 2024 |
| Assertio Therapeutics, Inc. | 2 | capsule, liquid filled; powder, for solution | New drug applications (NDA) | March 10, 2016 |
| Bryant Ranch Prepack | 2 | capsule, liquid filled; tablet, film coated | Generic drugs (ANDA) | March 24, 2022 |
| Carwin Pharmaceutical Associates, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 1, 2023 |
| Leading Pharma, LLC | 2 | powder, for solution; capsule, liquid filled | Authorized generics (NDA) | December 20, 2022 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet, coated; tablet, film coated | Generic drugs (ANDA) | September 15, 2021 |
| Phoenix RX LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 1, 2024 |
| Preferred Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 30, 2025 |
| Sola Pharmaceuticals, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 1, 2024 |
| A-S Medication Solutions | 1 | tablet, coated | Generic drugs (ANDA) | December 19, 2020 |
| Archis Pharma LLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 15, 2021 |
| Ascend Laboratories, LLC | 1 | powder, for solution | Generic drugs (ANDA) | October 24, 2022 |
| Assertio Specialty Pharmaceuticals LLC | 1 | capsule, liquid filled | New drug applications (NDA) | August 24, 2026 |
| Aurobindo Pharma Limited | 1 | capsule, liquid filled | Generic drugs (ANDA) | March 14, 2022 |
| AvKARE | 1 | tablet, film coated | Generic drugs (ANDA) | September 11, 2024 |
| Camber Pharmaceuticals, Inc. | 1 | powder, for solution | Generic drugs (ANDA) | March 4, 2022 |
| Chartwell RX, LLC | 1 | capsule, liquid filled | Generic drugs (ANDA) | November 21, 2022 |
| Coupler LLC | 1 | tablet, coated | Generic drugs (ANDA) | February 24, 2025 |
| Doc Rx | 1 | tablet, film coated | Generic drugs (ANDA) | October 21, 2024 |
| Golden State Medical Supply, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 18, 2004 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 1 | capsule, liquid filled | Generic drugs (ANDA) | November 21, 2022 |
| Ina Pharmaceutics Inc | 1 | tablet, coated | Generic drugs (ANDA) | September 20, 2021 |
| Ingenus Pharmaceuticals, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | October 11, 2021 |
| Lifsa Drugs LLC | 1 | capsule, liquid filled | Generic drugs (ANDA) | May 1, 2025 |
| Marlex Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 1, 2025 |
| Nivagen Pharmaceuticals, Inc. | 1 | powder, for solution | Generic drugs (ANDA) | December 15, 2025 |
| Northwind Health Company, LLC | 1 | tablet, coated | Generic drugs (ANDA) | October 27, 2022 |
| NuCare Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 11, 1998 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 11, 1998 |
| Par Health USA, LLC | 1 | powder, for solution | Generic drugs (ANDA) | January 3, 2023 |
| Proficient Rx LP | 1 | tablet, coated | Generic drugs (ANDA) | December 19, 2020 |
| Remedyrepack Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | September 26, 2022 |
| Strides Pharma Science Limited | 1 | capsule, liquid filled | Generic drugs (ANDA) | September 20, 2022 |
| Sun Pharmaceutical Industries, Inc. | 1 | powder, for solution | Generic drugs (ANDA) | June 24, 2024 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | August 11, 1998 |
| Teva Pharmaceuticals, Inc. | 1 | capsule, liquid filled | Generic drugs (ANDA) | March 24, 2022 |
| Torrent Pharmaceuticals Limited | 1 | powder, for solution | Generic drugs (ANDA) | January 22, 2025 |
| Trifluent Pharma, LLC | 1 | tablet, coated | Generic drugs (ANDA) | February 17, 2023 |
| Umedica Laboratories USA Inc. | 1 | powder, for solution | Generic drugs (ANDA) | February 15, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 25 | 44.6% |
| Capsule, liquid filled | 11 | 19.6% |
| Tablet, coated | 11 | 19.6% |
| Powder, for solution | 9 | 16.1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 50 | 89.3% |
| New drug applications (NDA) | 3 | 5.4% |
| Authorized generics (NDA) | 3 | 5.4% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 56 |
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.