Data / Drug companies / Letrozole
Letrozole: 17 companies and 19 products in the FDA NDC directory
Letrozole is listed in the FDA National Drug Code Directory by 17 companies, with 19 products in commercial distribution. 18 of the products (94.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on June 30, 2026.
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- Companies listing it
- 17
- Products
- 19
- Generic (ANDA) products
- 18 (94.7%)
- Application numbers
- 7
- Routes
- Oral
- Brand names
- Femara
- openFDA record search
- api.fda.gov
Companies that list letrozole
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 2 | tablet; tablet, film coated | Generic drugs (ANDA) | June 4, 2011 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 2, 2011 |
| Accord Healthcare Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | June 2, 2011 |
| Atlantic Biologicals Corp. | 1 | tablet, film coated | Generic drugs (ANDA) | January 13, 2020 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | January 11, 2019 |
| AvKARE | 1 | tablet, film coated | Generic drugs (ANDA) | January 5, 2015 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | October 2, 2019 |
| Breckenridge Pharmaceutical, Inc. | 1 | tablet | Generic drugs (ANDA) | June 4, 2011 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | June 2, 2011 |
| Bryant Ranch Prepack | 1 | tablet | Generic drugs (ANDA) | June 4, 2011 |
| Carnegie Pharmaceuticals LLC | 1 | tablet, film coated | Generic drugs (ANDA) | June 30, 2026 |
| Chartwell RX, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | May 9, 2019 |
| Dr. Reddy's Laboratories Limited | 1 | tablet, film coated | Generic drugs (ANDA) | June 3, 2011 |
| Natco Pharma Limited | 1 | tablet | Generic drugs (ANDA) | June 3, 2011 |
| Novartis Pharmaceuticals Corporation | 1 | tablet, film coated | New drug applications (NDA) | July 31, 1997 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | June 3, 2011 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | June 3, 2011 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 14 | 73.7% |
| Tablet | 5 | 26.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 18 | 94.7% |
| New drug applications (NDA) | 1 | 5.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Aromatase Inhibitor | 19 |
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.