Data / Drug companies / Cefaclor
Cefaclor: 4 companies and 5 products in the FDA NDC directory
Cefaclor is listed in the FDA National Drug Code Directory by 4 companies, with 5 products in commercial distribution. 5 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; tablet, film coated, extended release; suspension, and the newest product started marketing on November 1, 2022.
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- Companies listing it
- 4
- Products
- 5
- Generic (ANDA) products
- 5 (100.0%)
- Application numbers
- 3
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list cefaclor
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Carlsbad Technology, Inc. | 2 | capsule | Generic drugs (ANDA) | July 31, 2008 |
| A-S Medication Solutions | 1 | capsule | Generic drugs (ANDA) | July 31, 2008 |
| Azorian Pharma, LLC | 1 | suspension | Generic drugs (ANDA) | November 1, 2022 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | September 26, 2002 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 3 | 60% |
| Tablet, film coated, extended release | 1 | 20% |
| Suspension | 1 | 20% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 5 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cephalosporin Antibacterial | 5 |
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.