Quick answers
- What is Miudella?
- Miudella is a brand name of Copper, a prescription medicine. The FDA NDC Directory lists 1 Miudella product in 1 strength and form.
- Who makes Miudella?
- Sebela Womens Hlth holds the FDA application for Miudella (NDA218201, approved February 24, 2025).
- Is there a generic or store brand of Miudella?
- Other products of Copper are listed with the FDA, but none in exactly the same strength and form as a Miudella product.
- Has Miudella been recalled?
- No recall linked to Miudella products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Miudella is
Each Miudella 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.
Copper · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| copper 175 mm intrauterine device (intrauterine) | Miudella | None listed | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Copper →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA218201 | Sebela Womens Hlth | February 24, 2025 | 1 |
Companies that list Miudella
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Miudella products.
- Organon LLC1 product
Recalls
No recall linked to Miudella 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.