Quick answers
- What is Etyqa?
- Etyqa is a brand name of Estradiol and norethindrone acetate, a prescription medicine. The FDA NDC Directory lists 2 Etyqa products in 2 strengths and forms.
- Who makes Etyqa?
- Aurobindo Pharma Ltd holds the FDA application for Etyqa (ANDA214729, approved June 30, 2023).
- Is there a generic or store brand of Etyqa?
- Yes. The FDA NDC Directory lists 10 other products with the same active ingredients, strength and form as a Etyqa product, 6 of them generic. Ask your pharmacist whether one is right for you.
- Has Etyqa been recalled?
- No recall linked to Etyqa products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Etyqa is
Each Etyqa product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Estradiol and norethindrone acetate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| estradiol 0.5 mg · norethindrone acetate 0.1 mg tablet, film coated (oral) | Etyqa | 4 products, 3 companies | DailyMed |
| estradiol 1 mg · norethindrone acetate 0.5 mg tablet, film coated (oral) | Etyqa | 6 products, 5 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Estradiol and norethindrone acetate →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA214729 | Aurobindo Pharma Ltd | June 30, 2023 | 2 |
Companies that list Etyqa
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Etyqa products.
- Aurobindo Pharma Limited2 products
Recalls
No recall linked to Etyqa products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.