Data / Drug companies / Flucytosine
Flucytosine: 10 companies and 20 products in the FDA NDC directory
Flucytosine is listed in the FDA National Drug Code Directory by 10 companies, with 20 products in commercial distribution. 18 of the products (90.0%) 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 July 24, 2025.
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- Companies listing it
- 10
- Products
- 20
- Generic (ANDA) products
- 18 (90.0%)
- Application numbers
- 6
- Routes
- Oral
- Brand names
- Ancobon
- openFDA record search
- api.fda.gov
Companies that list flucytosine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| American Health Packaging | 2 | capsule | Generic drugs (ANDA) | December 17, 2021 |
| Aurobindo Pharma Limited | 2 | capsule | Generic drugs (ANDA) | May 1, 2020 |
| AvPAK | 2 | capsule | Generic drugs (ANDA) | April 12, 2021 |
| Bausch Health US LLC | 2 | capsule | New drug applications (NDA) | November 26, 1971 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 2 | capsule | Generic drugs (ANDA) | June 25, 2023 |
| Laurus Labs Limited | 2 | capsule | Generic drugs (ANDA) | July 24, 2025 |
| Lupin Pharmaceuticals,Inc. | 2 | capsule | Generic drugs (ANDA) | July 7, 2017 |
| Major Pharmaceuticals | 2 | capsule | Generic drugs (ANDA) | July 7, 2017 |
| Novel Laboratories, Inc. | 2 | capsule | Generic drugs (ANDA) | July 7, 2017 |
| Sigmapharm Laboratories, LLC | 2 | capsule | Generic drugs (ANDA) | June 1, 2018 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 20 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 18 | 90% |
| New drug applications (NDA) | 2 | 10% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nucleoside Analog Antifungal | 20 |
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.