Data / Drug companies / Dronabinol
Dronabinol: 7 companies and 15 products in the FDA NDC directory
Dronabinol is listed in the FDA National Drug Code Directory by 7 companies, with 15 products in commercial distribution. 3 of the products (20.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; solution, and the newest product started marketing on April 16, 2026.
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- Companies listing it
- 7
- Products
- 15
- Generic (ANDA) products
- 3 (20.0%)
- Application numbers
- 3
- Controlled substance schedule
- Schedule II, Schedule III
- Routes
- Oral
- Brand names
- Marinol, Syndros
- openFDA record search
- api.fda.gov
Companies that list dronabinol
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Ascend Laboratories, LLC | 3 | capsule | Authorized generics (NDA) | March 3, 2021 |
| Camber Pharmaceuticals, Inc. | 3 | capsule | Generic drugs (ANDA) | February 10, 2020 |
| ThePharmaNetwork, LLC | 3 | capsule | New drug applications (NDA) | March 3, 2021 |
| Major Pharmaceuticals | 2 | capsule | Authorized generics (NDA) | March 3, 2021 |
| Wellhouse Pharma, LLC | 2 | solution | New drug applications (NDA) | April 16, 2026 |
| Benuvia Operations, LLC | 1 | solution | New drug applications (NDA) | July 1, 2017 |
| Chartwell RX, LLC | 1 | solution | New drug applications (NDA) | July 1, 2017 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 11 | 73.3% |
| Solution | 4 | 26.7% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 7 | 46.7% |
| Authorized generics (NDA) | 5 | 33.3% |
| Generic drugs (ANDA) | 3 | 20% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cannabinoid | 15 |
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.