Class III · Low risk
Sodium Iodide I 131 Capsule
Labeling: Label Error on Declared Strength
National Drug Code
Is NDC 65174-0461-05 recalled?
Sodium Iodide I 131 Diagnostic · 5 CAPSULE in 1 VIAL (65174-461-05)
Yes — this exact package was recalled
1 FDA recall names the code 65174-0461-05 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Sodium Iodide I 131
- Strength
- SODIUM IODIDE I-131 100 mCi/1
- Form
- Capsule · Oral
- Labeler
- Jubilant DraxImage Inc., dba Jubilant Radiopharma
- Type
- Human Prescription Drug
- Product code
- 65174-0461
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 65174-0179 Kit for the Preparation of Technetium Tc 99m Sulfur Colloid 1
- 65174-0270 Draximage Maa 1
- 65174-0288 Draximage Dtpa 1
Free recall alerts
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