Quick answers
- What is ParaGard T 380A?
- ParaGard T 380A is a brand name of Copper, a prescription medicine. The FDA NDC Directory lists 2 ParaGard T 380A products in 1 strength and form.
- Who makes ParaGard T 380A?
- Coopersurgical holds the FDA application for ParaGard T 380A (NDA018680, approved November 15, 1984).
- Is there a generic or store brand of ParaGard T 380A?
- Other products of Copper are listed with the FDA, but none in exactly the same strength and form as a ParaGard T 380A product.
- Has ParaGard T 380A been recalled?
- No recall linked to ParaGard T 380A products (by their NDC code or label) appears in the FDA enforcement reports we use.
What ParaGard T 380A is
Each ParaGard T 380A 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 313.4 mg intrauterine device (intrauterine) | ParaGard T 380A | None listed | DailyMed |
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 |
|---|---|---|---|
| NDA018680 | Coopersurgical | November 15, 1984 | 2 |
Companies that list ParaGard T 380A
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of ParaGard T 380A products.
- CooperSurgical, Inc.2 products
Recalls
No recall linked to ParaGard T 380A 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.