Data / Drug companies / Cefixime
Cefixime: 7 companies and 12 products in the FDA NDC directory
Cefixime is listed in the FDA National Drug Code Directory by 7 companies, with 12 products in commercial distribution. 10 of the products (83.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; powder, for suspension; tablet, and the newest product started marketing on September 21, 2026.
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- Companies listing it
- 7
- Products
- 12
- Generic (ANDA) products
- 10 (83.3%)
- Application numbers
- 7
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list cefixime
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Lupin Pharmaceuticals, Inc. | 3 | powder, for suspension; capsule | Generic drugs (ANDA) | October 14, 2020 |
| Remedyrepack Inc. | 3 | capsule | Generic drugs (ANDA) | September 21, 2026 |
| Aurobindo Pharma Limited | 2 | powder, for suspension | Generic drugs (ANDA) | April 14, 2015 |
| Ascend Laboratories, LLC | 1 | capsule | Generic drugs (ANDA) | October 12, 2018 |
| Aurobindo Pharma Limited | 1 | capsule | Generic drugs (ANDA) | March 23, 2026 |
| Health Department, Oklahoma State | 1 | capsule | Generic drugs (ANDA) | October 12, 2018 |
| Rising Pharma Holdings, Inc. | 1 | tablet | Generic drugs (ANDA) | December 12, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 7 | 58.3% |
| Powder, for suspension | 4 | 33.3% |
| Tablet | 1 | 8.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 10 | 83.3% |
| Authorized generics (NDA) | 2 | 16.7% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cephalosporin Antibacterial | 12 |
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.