Data / Drug companies / Lundbeck Pharmaceuticals LLC
Lundbeck Pharmaceuticals LLC: 11 products in the FDA NDC directory, labeler code 67386
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Lundbeck Pharmaceuticals LLC (labeler code 67386) lists 11 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 11 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on February 21, 2020.
The request: Watch Lundbeck Pharmaceuticals LLC (FDA labeler code 67386): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 67386
- Products in commercial distribution
- 11
- Packages
- 12
- Finished drugs by generic name
- 5
- Prescription products
- 11
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 3
- Flagged as original packager
- 6 of 6 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 24, 2008
- 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) | 10 | 90.9% |
| Biologics (BLA) | 1 | 9.1% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 11 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Droxidopa | 3 | 15 |
| Clobazam | 3 | 18 |
| Vigabatrin | 2 | 18 |
| Tetrabenazine | 2 | 12 |
| Eptinezumab-jjmr | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 36.4% |
| Capsule | 3 | 27.3% |
| Tablet, film coated | 1 | 9.1% |
| Injection | 1 | 9.1% |
| Suspension | 1 | 9.1% |
| Powder, for solution | 1 | 9.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Benzodiazepine | 3 |
| Anti-epileptic Agent | 2 |
| Vesicular Monoamine Transporter 2 Inhibitor | 2 |
| Calcitonin Gene-related Peptide Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Vyepti | 67386-130 | Injection | Biologics (BLA) | February 21, 2020 |
| Northera | 67386-822 | Capsule | New drug applications (NDA) | September 1, 2014 |
| Northera | 67386-821 | Capsule | New drug applications (NDA) | September 1, 2014 |
| Northera | 67386-820 | Capsule | New drug applications (NDA) | September 1, 2014 |
| Onfi | 67386-315 | Tablet | New drug applications (NDA) | December 10, 2013 |
| Onfi | 67386-314 | Tablet | New drug applications (NDA) | December 10, 2013 |
| Onfi | 67386-313 | Suspension | New drug applications (NDA) | December 14, 2012 |
| Sabril | 67386-211 | Powder, for solution | New drug applications (NDA) | August 21, 2009 |
| Sabril | 67386-111 | Tablet, film coated | New drug applications (NDA) | August 21, 2009 |
| Xenazine | 67386-422 | Tablet | New drug applications (NDA) | November 24, 2008 |
| Xenazine | 67386-421 | Tablet | New drug applications (NDA) | November 24, 2008 |
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.