Data / Drug companies / Cyproheptadine hydrochloride
Cyproheptadine hydrochloride: 24 companies and 38 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Cyproheptadine hydrochloride is listed in the FDA National Drug Code Directory by 24 companies, with 38 products in commercial distribution. 38 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; solution; syrup, and the newest product started marketing on October 15, 2026.
The request: Get every company that lists cyproheptadine hydrochloride in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Companies listing it
- 24
- Products
- 38
- Generic (ANDA) products
- 38 (100.0%)
- Application numbers
- 14
- Routes
- Oral
- Brand names
- Cyproheptadine
- openFDA record search
- api.fda.gov
Companies that list cyproheptadine hydrochloride
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 5 | tablet | Generic drugs (ANDA) | February 24, 2021 |
| Quagen Pharmaceuticals LLC | 4 | solution; tablet | Generic drugs (ANDA) | October 15, 2026 |
| A-S Medication Solutions | 2 | tablet | Generic drugs (ANDA) | July 20, 2017 |
| Atlantic Biologicals Corp. | 2 | solution; syrup | Generic drugs (ANDA) | December 22, 2023 |
| Bryant Ranch Prepack | 2 | tablet; solution | Generic drugs (ANDA) | February 24, 2021 |
| Chartwell RX, LLC | 2 | tablet; syrup | Generic drugs (ANDA) | July 13, 2017 |
| QPharma, Inc. | 2 | tablet | Generic drugs (ANDA) | February 24, 2021 |
| Remedyrepack Inc. | 2 | tablet | Generic drugs (ANDA) | May 27, 2026 |
| TruPharma, LLC | 2 | tablet | Generic drugs (ANDA) | June 1, 2026 |
| Amneal Pharmaceuticals of New York LLC | 1 | tablet | Generic drugs (ANDA) | July 29, 2015 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | October 30, 2025 |
| Cranbury Pharmaceuticals, LLC | 1 | syrup | Generic drugs (ANDA) | December 21, 2021 |
| Golden State Medical Supply, Inc. | 1 | tablet | Generic drugs (ANDA) | September 23, 2015 |
| Ingenus Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | September 23, 2015 |
| Method Pharmaceuticals, LLC | 1 | solution | Generic drugs (ANDA) | June 15, 2024 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | March 1, 2020 |
| Pangea Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | October 12, 2026 |
| Patrin Pharma, Inc. | 1 | solution | Generic drugs (ANDA) | February 15, 2022 |
| Rising Pharma Holdings, Inc. | 1 | tablet | Generic drugs (ANDA) | February 9, 2022 |
| Rising Pharma Holdings, Inc. | 1 | syrup | Generic drugs (ANDA) | July 10, 2006 |
| Strides Pharma Science Limited | 1 | tablet | Generic drugs (ANDA) | April 11, 2018 |
| Unichem Pharmaceuticals (USA), Inc. | 1 | tablet | Generic drugs (ANDA) | March 1, 2020 |
| Zydus Lifesciences Limited | 1 | tablet | Generic drugs (ANDA) | July 20, 2017 |
| Zydus Pharmaceuticals USA Inc. | 1 | tablet | Generic drugs (ANDA) | July 20, 2017 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 28 | 73.7% |
| Solution | 6 | 15.8% |
| Syrup | 4 | 10.5% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 38 | 100% |
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.