Data / Drug companies / Axsome Therapeutics, Inc.
Axsome Therapeutics, Inc.: 7 products in the FDA NDC directory, labeler code 81968
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Axsome Therapeutics, Inc. (labeler code 81968) lists 7 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 7 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on July 30, 2026.
The request: Watch Axsome Therapeutics, Inc. (FDA labeler code 81968): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 81968
- Products in commercial distribution
- 7
- Packages
- 17
- Finished drugs by generic name
- 3
- Prescription products
- 7
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 2
- Flagged as original packager
- 6 of 6 products that carry the flag
- Started marketing in the last 12 months
- 3
- Earliest marketing start
- June 18, 2019
- 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) | 7 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 7 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Dextromethorphan hydrobromide, bupropion hydrochloride | 4 | 1 |
| Solriamfetol | 2 | 1 |
| Meloxicam, rizatriptan | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 2 | 28.6% |
| Kit | 2 | 28.6% |
| Tablet, multilayer, extended release | 2 | 28.6% |
| Tablet | 1 | 14.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Dopamine and Norepinephrine Reuptake Inhibitor | 2 |
| Aminoketone | 2 |
| Sigma-1 Agonist | 2 |
| Uncompetitive N-methyl-D-aspartate Receptor Antagonist | 2 |
| Nonsteroidal Anti-inflammatory Drug | 1 |
| Serotonin-1b and Serotonin-1d Receptor Agonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Auvelity | 81968-453 | Kit | New drug applications (NDA) | July 30, 2026 |
| Auvelity | 81968-345 | Kit | New drug applications (NDA) | June 1, 2026 |
| Auvelity | 81968-030 | Tablet, multilayer, extended release | New drug applications (NDA) | May 8, 2026 |
| Symbravo | 81968-020 | Tablet | New drug applications (NDA) | May 19, 2025 |
| Auvelity | 81968-045 | Tablet, multilayer, extended release | New drug applications (NDA) | August 18, 2022 |
| Sunosi | 81968-351 | Tablet, film coated | New drug applications (NDA) | June 18, 2019 |
| Sunosi | 81968-350 | Tablet, film coated | New drug applications (NDA) | June 18, 2019 |
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.