Amlodipine Besylate And Benazepril Hydrochloride recalls
Amlodipine Besylate And Benazepril Hydrochloride products have been recalled 2 times, most recently on 6 Aug 2025. The recalling company is usually Lupin Pharmaceuticals. The most common reason is labeling errors.
Total recalls2since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 6 Aug 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why amlodipine besylate and benazepril hydrochloride is recalled
Companies
Product types
By year
All amlodipine besylate and benazepril hydrochloride recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg recalledAmlodipine Besylate And Benazepril Hydrochloride | Lupin Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Dr. Reddy's Amlodipine Besylate recalledAmlodipine Besylate And Benazepril Hydrochloride | Dr. Reddy's Laboratories | Labeling Errors | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.