Data / Drug companies / Factor VIII Activator
Factor VIII Activator drugs: 2 drugs from 28 companies in the FDA NDC directory
Factor VIII Activator is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 58 products in this class from 28 companies, covering 2 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 30, 2026.
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- 28Companies
- 58Products
- 2Drugs by generic name
Drugs in the Factor VIII Activator class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Desmopressin acetate | 57 | 27 |
| Desmopressin acetate oral solution | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Nordic Pharma, Inc. | 7 | solution; tablet | New drug applications (NDA) | May 9, 2022 |
| Ferring Pharmaceuticals Inc. | 5 | tablet; injection | New drug applications (NDA) | June 25, 2025 |
| Apotex Corp. | 3 | tablet; spray | Generic drugs (ANDA) | November 30, 2020 |
| Ubi Pharma Inc. | 3 | injection | Generic drugs (ANDA) | September 17, 2020 |
| American Health Packaging | 2 | tablet | Generic drugs (ANDA) | February 16, 2024 |
| Armas Pharmaceuticals Inc. | 2 | injection, solution | Generic drugs (ANDA) | June 30, 2026 |
| Aurobindo Pharma Limited | 2 | tablet | Generic drugs (ANDA) | March 21, 2024 |
| BluePoint Laboratories | 2 | tablet | Generic drugs (ANDA) | August 3, 2023 |
| Caplin Steriles Limited | 2 | injection, solution | Generic drugs (ANDA) | March 16, 2026 |
| Dr. Reddy's Laboratories Inc. | 2 | injection; injection, solution | Generic drugs (ANDA) | September 12, 2022 |
| Fresenius Kabi USA, LLC | 2 | injection, solution | Generic drugs (ANDA) | September 11, 2023 |
| Gland Pharma Limited | 2 | injection, solution | Generic drugs (ANDA) | March 20, 2023 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 2 | tablet | Generic drugs (ANDA) | May 26, 2017 |
| KVK-Tech, Inc. | 2 | tablet | Generic drugs (ANDA) | January 28, 2019 |
| Meitheal Pharmaceuticals Inc. | 2 | injection | Generic drugs (ANDA) | February 13, 2026 |
| Sagent Pharmaceuticals | 2 | injection, solution | Generic drugs (ANDA) | March 15, 2018 |
| Sun Pharmaceutical Industries, Inc. | 2 | injection, solution | Generic drugs (ANDA) | February 20, 2014 |
| Sun Pharmaceutical Industries, Inc. | 2 | injection, solution | Generic drugs (ANDA) | June 20, 2023 |
| The J. Molner Company LLC | 2 | injection, solution | Generic drugs (ANDA) | October 30, 2026 |
| XGen Pharmaceuticals DJB, Inc. | 2 | injection, solution | Generic drugs (ANDA) | March 22, 2024 |
| Avenacy, LLC | 1 | injection, solution | Generic drugs (ANDA) | January 15, 2024 |
| Bausch & Lomb Incorporated | 1 | solution | Generic drugs (ANDA) | January 25, 1999 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | March 7, 2006 |
| Bryant Ranch Prepack | 1 | tablet | New drug applications (NDA) | December 10, 2015 |
| Eton Pharmaceuticals, Inc. | 1 | solution | New drug applications (NDA) | March 2, 2026 |
| Northwind Health Company, LLC | 1 | tablet | Generic drugs (ANDA) | October 29, 2020 |
| Oceanside Pharmaceuticals | 1 | solution | Generic drugs (ANDA) | June 1, 2025 |
| Remedyrepack Inc. | 1 | tablet | Generic drugs (ANDA) | April 23, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 20 | 34.5% |
| Tablet | 20 | 34.5% |
| Solution | 8 | 13.8% |
| Injection | 8 | 13.8% |
| Spray | 2 | 3.4% |
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.