Class II ยท Moderate risk
Carisoprodol Tablets
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
National Drug Code
Is NDC 0591-5513-05 recalled?
Carisoprodol
Yes — this exact package was recalled
1 FDA recall names the code 0591-5513-05 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
- Carisoprodol
- Strength
- CARISOPRODOL 350 mg/1
- Form
- Tablet
- Labeler
- Actavis Pharma, Inc.
- Type
- Drug for Further Processing · DEA CIV
- Product code
- 0591-5513
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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