Data / Drug companies / Supernus Pharmaceuticals, Inc.
Supernus Pharmaceuticals, Inc.: 12 products in the FDA NDC directory, labeler code 17772
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Supernus Pharmaceuticals, Inc. (labeler code 17772) lists 12 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 12 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on April 2, 2021.
The request: Watch Supernus Pharmaceuticals, Inc. (FDA labeler code 17772): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 17772
- Products in commercial distribution
- 12
- Packages
- 48
- Finished drugs by generic name
- 4
- Prescription products
- 12
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 17, 2013
- 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) | 12 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 12 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Topiramate | 4 | 56 |
| Viloxazine hydrochloride | 3 | 1 |
| Oxcarbazepine | 3 | 46 |
| Amantadine | 2 | 10 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule, extended release | 7 | 58.3% |
| Tablet | 3 | 25% |
| Capsule, coated pellets | 2 | 16.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Norepinephrine Reuptake Inhibitor | 3 |
| Anti-epileptic Agent | 3 |
| Influenza A M2 Protein Inhibitor | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Qelbree | 17772-133 | Capsule, extended release | New drug applications (NDA) | April 2, 2021 |
| Qelbree | 17772-132 | Capsule, extended release | New drug applications (NDA) | April 2, 2021 |
| Qelbree | 17772-131 | Capsule, extended release | New drug applications (NDA) | April 2, 2021 |
| Gocovri | 17772-170 | Capsule, coated pellets | New drug applications (NDA) | August 24, 2017 |
| Gocovri | 17772-085 | Capsule, coated pellets | New drug applications (NDA) | August 24, 2017 |
| Trokendi XR | 17772-104 | Capsule, extended release | New drug applications (NDA) | August 16, 2013 |
| Trokendi XR | 17772-103 | Capsule, extended release | New drug applications (NDA) | August 16, 2013 |
| Trokendi XR | 17772-102 | Capsule, extended release | New drug applications (NDA) | August 16, 2013 |
| Trokendi XR | 17772-101 | Capsule, extended release | New drug applications (NDA) | August 16, 2013 |
| Oxtellar xr | 17772-123 | Tablet | New drug applications (NDA) | January 17, 2013 |
| Oxtellar xr | 17772-122 | Tablet | New drug applications (NDA) | January 17, 2013 |
| Oxtellar xr | 17772-121 | Tablet | New drug applications (NDA) | January 17, 2013 |
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.