Data / Drug companies / Diclofenac potassium, film coated
Diclofenac potassium, film coated: 8 companies and 8 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Diclofenac potassium, film coated is listed in the FDA National Drug Code Directory by 8 companies, with 8 products in commercial distribution. 8 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on July 26, 2026.
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- Companies listing it
- 8
- Products
- 8
- Generic (ANDA) products
- 8 (100.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Diclofenac Potassium
- openFDA record search
- api.fda.gov
Companies that list diclofenac potassium, film coated
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Amerisyn LLC | 1 | tablet | Generic drugs (ANDA) | July 26, 2026 |
| Amici Pharma, Inc. | 1 | tablet | Generic drugs (ANDA) | March 12, 2024 |
| Cintex Services, LLC | 1 | tablet | Generic drugs (ANDA) | December 19, 2023 |
| Golden State Medical Supply, Inc. | 1 | tablet | Generic drugs (ANDA) | March 15, 2023 |
| Happy Robin, LLC | 1 | tablet | Generic drugs (ANDA) | September 24, 2025 |
| Havix Group Inc D-B-A Aavis Pharmaceuticals | 1 | tablet | Generic drugs (ANDA) | June 25, 2023 |
| Ina Pharmaceutics Inc | 1 | tablet | Generic drugs (ANDA) | October 1, 2024 |
| Vici Pharmaceuticals, Inc | 1 | tablet | Generic drugs (ANDA) | June 10, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 8 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 8 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 8 |
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.