Data / Drug companies / Raloxifene hydrochloride
Raloxifene hydrochloride: 16 companies and 19 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Raloxifene hydrochloride is listed in the FDA National Drug Code Directory by 16 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, coated; tablet, and the newest product started marketing on June 27, 2018.
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- Companies listing it
- 16
- Products
- 19
- Generic (ANDA) products
- 18 (94.7%)
- Application numbers
- 7
- Routes
- Oral
- Brand names
- Evista
- openFDA record search
- api.fda.gov
Companies that list raloxifene 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 | 3 | tablet, film coated | Generic drugs (ANDA) | October 12, 2016 |
| A-S Medication Solutions | 2 | tablet, coated; tablet, film coated | Generic drugs (ANDA) | December 30, 2017 |
| Amneal Pharmaceuticals LLC | 1 | tablet, film coated | Generic drugs (ANDA) | January 20, 2016 |
| Aphena Pharma Solutions - Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | October 12, 2016 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | August 28, 2015 |
| AvPAK | 1 | tablet, film coated | Generic drugs (ANDA) | June 27, 2018 |
| Bryant Ranch Prepack | 1 | tablet, coated | Generic drugs (ANDA) | December 30, 2017 |
| Cadila Pharmaceuticals Limited | 1 | tablet, coated | Generic drugs (ANDA) | December 30, 2017 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 12, 2016 |
| Eli Lilly and Company | 1 | tablet | New drug applications (NDA) | January 6, 1998 |
| Exelan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | November 12, 2014 |
| Major Pharmaceuticals | 1 | tablet, film coated | Generic drugs (ANDA) | October 12, 2016 |
| Modavar Pharmaceuticals LLC | 1 | tablet, coated | Generic drugs (ANDA) | December 30, 2017 |
| NorthStar Rx LLC | 1 | tablet, film coated | Generic drugs (ANDA) | August 28, 2015 |
| ScieGen Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 12, 2016 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 28, 2014 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 14 | 73.7% |
| Tablet, coated | 4 | 21.1% |
| Tablet | 1 | 5.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 18 | 94.7% |
| New drug applications (NDA) | 1 | 5.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Estrogen Agonist/Antagonist | 19 |
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.