Quick answers
- What is Sodium Iodide I 131 Diagnostic?
- Sodium Iodide I 131 Diagnostic is a brand name of Sodium iodide i 131, a prescription medicine. The FDA NDC Directory lists 1 Sodium Iodide I 131 Diagnostic product in 1 strength and form.
- Who makes Sodium Iodide I 131 Diagnostic?
- Jubilant holds the FDA application for Sodium Iodide I 131 Diagnostic (NDA021305, approved January 24, 2003).
- Is there a generic or store brand of Sodium Iodide I 131 Diagnostic?
- Other products of Sodium iodide i 131 are listed with the FDA, but none in exactly the same strength and form as a Sodium Iodide I 131 Diagnostic product.
- Has Sodium Iodide I 131 Diagnostic been recalled?
- FDA enforcement reports list 1 recall of Sodium Iodide I 131 Diagnostic products; the newest started March 11, 2016. A recall usually concerns specific lots, not every product.
What Sodium Iodide I 131 Diagnostic is
Each Sodium Iodide I 131 Diagnostic 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.
Sodium iodide i 131 · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| sodium iodide I-131 100 mCi capsule (oral) | Sodium Iodide I 131 Diagnostic | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Sodium iodide i 131 →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021305 | Jubilant | January 24, 2003 | 1 |
Companies that list Sodium Iodide I 131 Diagnostic
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Sodium Iodide I 131 Diagnostic products.
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
March 11, 2016 · Class III · Terminated · D-0812-2016
Labeling: Label Error on Declared Strength
SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, Canada, NDC 65174-461-05 — Jubilant Draximage Inc
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.