Class II ยท Moderate risk
Xanax XR
Failed Dissolution Specifications
National Drug Code
Is NDC 58151-0506-91 recalled?
Xanax XR · 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (58151-506-91)
Yes — this exact package was recalled
1 FDA recall names the code 58151-0506-91 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.
1 of these recalls is still ongoing.
- Active ingredient
- alprazolam
- Strength
- ALPRAZOLAM 3 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Viatris Specialty LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 58151-0506
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
- 58151-0078 Cardura XL 1
- 58151-0079 Cardura XL 1
Free recall alerts
Know the day your medication is recalled
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