Data / Drug companies / Ucb, Inc.
Ucb, Inc.: 6 products in the FDA NDC directory, labeler code 0131
Ucb, Inc. (labeler code 0131) lists 6 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 6 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on April 20, 2010.
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- Labeler code
- 0131
- Products in commercial distribution
- 6
- Packages
- 14
- Finished drugs by generic name
- 1
- Prescription products
- 6
- Over the counter products
- 0
- Controlled substance products
- Schedule V 6
- Flagged as original packager
- 6 of 6 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- May 26, 2009
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 6 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 6 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Lacosamide | 6 | 57 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 4 | 66.7% |
| Injection | 1 | 16.7% |
| Solution | 1 | 16.7% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Vimpat | 0131-5410 | Solution | New drug applications (NDA) | April 20, 2010 |
| Vimpat | 0131-2480 | Tablet, film coated | New drug applications (NDA) | May 26, 2009 |
| Vimpat | 0131-2479 | Tablet, film coated | New drug applications (NDA) | May 26, 2009 |
| Vimpat | 0131-2478 | Tablet, film coated | New drug applications (NDA) | May 26, 2009 |
| Vimpat | 0131-2477 | Tablet, film coated | New drug applications (NDA) | May 26, 2009 |
| Vimpat | 0131-1810 | Injection | New drug applications (NDA) | May 26, 2009 |
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.