Class I ยท High risk
Isovue -370
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
National Drug Code
Is NDC 0270-1316-67 recalled?
Isovue 370
Yes — this exact package was recalled
1 FDA recall names the code 0270-1316-67 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
- Iopamidol
- Strength
- IOPAMIDOL 755 mg/mL
- Form
- Injection, Solution · Intravascular
- Labeler
- Bracco Diagnostics Inc
- Type
- Human Prescription Drug
- Product code
- 0270-1316
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
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