Data / Drug companies / Voriconazole
Voriconazole: 34 companies and 56 products in the FDA NDC directory
Voriconazole is listed in the FDA National Drug Code Directory by 34 companies, with 56 products in commercial distribution. 49 of the products (87.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; injection, powder, lyophilized, for solution; powder, for suspension, and the newest product started marketing on August 27, 2026.
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- Companies listing it
- 34
- Products
- 56
- Generic (ANDA) products
- 49 (87.5%)
- Application numbers
- 24
- Routes
- Oral, Intravenous
- Brand names
- Vfend
- openFDA record search
- api.fda.gov
Companies that list voriconazole
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Roerig | 5 | injection, powder, lyophilized, for solution; tablet, film coated | New drug applications (NDA) | October 24, 2012 |
| American Health Packaging | 3 | tablet, film coated | Generic drugs (ANDA) | August 27, 2026 |
| Lupin Pharmaceuticals,Inc. | 3 | tablet, film coated; powder, for suspension | Generic drugs (ANDA) | June 1, 2016 |
| Sandoz Inc | 3 | tablet, film coated; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | May 30, 2012 |
| Ajanta Pharma USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | May 31, 2016 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | January 22, 2016 |
| Camber Pharmaceuticals, Inc. | 2 | injection, powder, lyophilized, for solution; powder, for suspension | Generic drugs (ANDA) | August 8, 2025 |
| Major Pharmaceuticals | 2 | tablet, film coated | Generic drugs (ANDA) | May 31, 2016 |
| Mylan Institutional Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | August 8, 2011 |
| Mylan Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | February 15, 2011 |
| NorthStar Rx LLC | 2 | tablet, film coated | Generic drugs (ANDA) | January 22, 2016 |
| Safecor Health, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | April 6, 2026 |
| Slate Run Pharmaceuticals, LLC | 2 | powder, for suspension; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | March 1, 2024 |
| Solco Healthcare US, LLC | 2 | tablet, coated | Generic drugs (ANDA) | October 28, 2016 |
| Viona Pharmaceuticals Inc | 2 | tablet, film coated | Generic drugs (ANDA) | April 16, 2019 |
| Zydus Lifesciences Limited | 2 | tablet, film coated | Generic drugs (ANDA) | May 25, 2016 |
| Amneal Pharmaceuticals LLC | 1 | powder, for suspension | Generic drugs (ANDA) | November 29, 2013 |
| AvPAK | 1 | tablet, coated | Generic drugs (ANDA) | August 19, 2022 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | May 13, 2025 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | December 12, 2011 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | December 12, 2011 |
| Civica, Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | April 1, 2023 |
| Eugia US LLC | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | February 2, 2023 |
| Fosun Pharma USA Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | January 4, 2021 |
| Fresenius Kabi USA, LLC | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | December 1, 2020 |
| Gland Pharma Limited | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | March 31, 2020 |
| Glenmark Pharmaceuticals Inc., USA | 1 | tablet, film coated | Generic drugs (ANDA) | September 4, 2015 |
| Hainan Poly Pharm. Co., Ltd. | 1 | injection, solution | Generic drugs (ANDA) | November 20, 2025 |
| Meitheal Pharmaceuticals Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | May 9, 2022 |
| Mylan Pharmaceuticals Inc. | 1 | powder, for suspension | Authorized generics (NDA) | December 16, 2013 |
| Novel Laboratories, Inc. | 1 | suspension | Generic drugs (ANDA) | June 1, 2016 |
| Ubi Pharma Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | August 31, 2020 |
| Xellia Pharmaceuticals USA LLC | 1 | injection, powder, lyophilized, for solution | New drug applications (NDA) | August 24, 2023 |
| Zhejiang Poly Pharm. Co., Ltd. | 1 | powder, for suspension | Generic drugs (ANDA) | April 11, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 30 | 53.6% |
| Injection, powder, lyophilized, for solution | 14 | 25% |
| Powder, for suspension | 7 | 12.5% |
| Tablet, coated | 3 | 5.4% |
| Suspension | 1 | 1.8% |
| Injection, solution | 1 | 1.8% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 49 | 87.5% |
| New drug applications (NDA) | 6 | 10.7% |
| Authorized generics (NDA) | 1 | 1.8% |
Pharmacologic classes
| Class | Products |
|---|---|
| Azole Antifungal | 56 |
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.