Data / Drug companies / Temazepam
Temazepam: 28 companies and 87 products in the FDA NDC directory
Temazepam is listed in the FDA National Drug Code Directory by 28 companies, with 87 products in commercial distribution. 74 of the products (85.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, and the newest product started marketing on February 19, 2024.
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- Companies listing it
- 28
- Products
- 87
- Generic (ANDA) products
- 74 (85.1%)
- Application numbers
- 8
- Controlled substance schedule
- Schedule IV
- Routes
- Oral
- Brand names
- Restoril
- openFDA record search
- api.fda.gov
Companies that list temazepam
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 9 | capsule | Generic drugs (ANDA) | June 28, 2012 |
| Bryant Ranch Prepack | 8 | capsule | Generic drugs (ANDA) | November 27, 2018 |
| SpecGx LLC | 8 | capsule | New drug applications (NDA) | February 23, 2010 |
| Alembic Pharmaceuticals Inc. | 4 | capsule | Generic drugs (ANDA) | November 27, 2018 |
| Alembic Pharmaceuticals Limited | 4 | capsule | Generic drugs (ANDA) | November 27, 2018 |
| Amneal Pharmaceuticals LLC | 4 | capsule | Generic drugs (ANDA) | May 23, 2016 |
| Aphena Pharma Solutions - Tennessee, LLC | 4 | capsule | New drug applications (NDA) | November 23, 2018 |
| Ascend Laboratories, LLC | 4 | capsule | Generic drugs (ANDA) | June 28, 2012 |
| Asclemed USA, Inc. | 4 | capsule | Generic drugs (ANDA) | June 28, 2012 |
| Bryant Ranch Prepack | 4 | capsule | Generic drugs (ANDA) | June 28, 2012 |
| Solco Healthcare US, LLC | 4 | capsule | Generic drugs (ANDA) | January 5, 2023 |
| Preferred Pharmaceuticals Inc. | 3 | capsule | Generic drugs (ANDA) | July 24, 2023 |
| A-S Medication Solutions | 2 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| Actavis Pharma, Inc. | 2 | capsule | Generic drugs (ANDA) | September 30, 1990 |
| Advanced Rx of Tennessee, LLC | 2 | capsule | Generic drugs (ANDA) | April 4, 2023 |
| Amneal Pharmaceuticals of New York LLC | 2 | capsule | Generic drugs (ANDA) | February 19, 2024 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| AvPAK | 2 | capsule | Generic drugs (ANDA) | October 19, 2023 |
| Golden State Medical Supply, Inc. | 2 | capsule | Generic drugs (ANDA) | November 23, 2018 |
| PD-Rx Pharmaceuticals, Inc. | 2 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| Proficient Rx LP | 2 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| Proficient Rx LP | 2 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| Remedyrepack Inc. | 2 | capsule | Generic drugs (ANDA) | December 16, 2019 |
| American Health Packaging | 1 | capsule | New drug applications (NDA) | August 1, 2012 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | capsule | Generic drugs (ANDA) | August 3, 1987 |
| Major Pharmaceuticals | 1 | capsule | Generic drugs (ANDA) | March 25, 2015 |
| NuCare Pharmaceuticals, Inc. | 1 | capsule | Generic drugs (ANDA) | April 21, 1987 |
| PD-Rx Pharmaceuticals, Inc. | 1 | capsule | New drug applications (NDA) | February 23, 2010 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 87 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 74 | 85.1% |
| New drug applications (NDA) | 13 | 14.9% |
Pharmacologic classes
| Class | Products |
|---|---|
| Benzodiazepine | 87 |
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.