Data / Drug companies / Ucb Pharma S.A.
Ucb Pharma S.A.: 20 products in the FDA NDC directory, labeler code 36998
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ucb Pharma S.A. (labeler code 36998) lists 20 products in the FDA National Drug Code Directory. By type: 17 drugs for further processing, 3 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on May 12, 2016.
The request: Watch Ucb Pharma S.A. (FDA labeler code 36998): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 36998
- Products in commercial distribution
- 20
- Packages
- 20
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Controlled substance products
- Schedule V 12
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- April 24, 2000
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Drugs for further processing | 17 | 85% |
| Bulk ingredients | 3 | 15% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 17 | 85% |
| Bulk ingredients | 3 | 15% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 13 | 65% |
| Powder | 3 | 15% |
| Tablet, film coated, extended release | 2 | 10% |
| Tablet, extended release | 1 | 5% |
| Injection, solution | 1 | 5% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Brivaracetam | 36998-4100 | Tablet, film coated | Drugs for further processing | May 12, 2016 |
| Brivaracetam | 36998-4000 | Tablet, film coated | Drugs for further processing | May 12, 2016 |
| Brivaracetam | 36998-3900 | Tablet, film coated | Drugs for further processing | May 12, 2016 |
| Brivaracetam | 36998-3800 | Tablet, film coated | Drugs for further processing | May 12, 2016 |
| Brivaracetam | 36998-3700 | Tablet, film coated | Drugs for further processing | May 12, 2016 |
| Brivaracetam | 36998-0118 | Powder | Bulk ingredients | May 26, 2015 |
| Lacosamide | 36998-2480 | Tablet, film coated | Drugs for further processing | May 26, 2009 |
| Lacosamide | 36998-2479 | Tablet, film coated | Drugs for further processing | May 26, 2009 |
| Lacosamide | 36998-2478 | Tablet, film coated | Drugs for further processing | May 26, 2009 |
| Lacosamide | 36998-2477 | Tablet, film coated | Drugs for further processing | May 26, 2009 |
| Lacosamide | 36998-1810 | Injection, solution | Drugs for further processing | May 26, 2009 |
| Lacosamide | 36998-0119 | Powder | Bulk ingredients | May 26, 2009 |
| Levetiracetam | 36998-5990 | Tablet, film coated, extended release | Drugs for further processing | April 1, 2009 |
| Levetiracetam | 36998-5980 | Tablet, film coated, extended release | Drugs for further processing | September 24, 2008 |
| Cetirizine hydrochloride and pseudoephedrine hydrochloride | 36998-9550 | Tablet, extended release | Drugs for further processing | August 10, 2001 |
| Levetiracetam | 36998-5970 | Tablet, film coated | Drugs for further processing | April 24, 2000 |
| Levetiracetam | 36998-5960 | Tablet, film coated | Drugs for further processing | April 24, 2000 |
| Levetiracetam | 36998-5950 | Tablet, film coated | Drugs for further processing | April 24, 2000 |
| Levetiracetam | 36998-5940 | Tablet, film coated | Drugs for further processing | April 24, 2000 |
| Levetiracetam | 36998-0117 | Powder | Bulk ingredients | April 24, 2000 |
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.