Class II ยท Moderate risk
Cardura XL
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
National Drug Code
Is NDC 58151-0078-93 recalled?
Cardura XL · 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58151-078-93)
Yes — this exact package was recalled
1 FDA recall names the code 58151-0078-93 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
- doxazosin mesylate
- Strength
- DOXAZOSIN MESYLATE 4 mg/1
- Form
- Tablet, Film Coated, Extended Release · Oral
- Labeler
- Viatris Specialty LLC
- Type
- Human Prescription Drug
- Product code
- 58151-0078
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
- 58151-0079 Cardura XL 1
- 58151-0506 Xanax XR 1
Free recall alerts
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