Data / Drug companies / Estradiol and norethindrone acetate
Estradiol and norethindrone acetate: 7 companies and 12 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Estradiol and norethindrone acetate is listed in the FDA National Drug Code Directory by 7 companies, with 12 products in commercial distribution. 12 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated, and the newest product started marketing on January 29, 2025.
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- Companies listing it
- 7
- Products
- 12
- Generic (ANDA) products
- 12 (100.0%)
- Application numbers
- 6
- Routes
- Oral
- Brand names
- Estradiol / Norethindrone Acetate, Etyqa, Mimvey, Abigale Lo, Abigale
- openFDA record search
- api.fda.gov
Companies that list estradiol and norethindrone acetate
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, film coated; tablet | Generic drugs (ANDA) | April 3, 2019 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | June 30, 2023 |
| Breckenridge Pharmaceutical, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 9, 2011 |
| Ingenus Pharmaceuticals, LLC | 2 | tablet | Generic drugs (ANDA) | April 3, 2019 |
| Xiromed, LLC | 2 | tablet | Generic drugs (ANDA) | January 29, 2025 |
| Naari Pte Limited | 1 | tablet | Generic drugs (ANDA) | June 11, 2024 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | June 2, 2010 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 6 | 50% |
| Tablet, film coated | 6 | 50% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 12 | 100% |
Pharmacologic classes
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.