FDA Drug recall D-1434-2012
Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd
- FDA Drug
- Class II
- terminated
- Published 2012-08-08
On 2012-08-08 the FDA classified a Class II recall of Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd by Dr Reddy S Laboratories, citing adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ci….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1434-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-09 |
| Published | 2012-08-08 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Dr Reddy S Laboratories |
| Distribution | US |
Product
Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-340-05
Reason
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets.
Identifiers
| ndc | 55111-338-30 |
|---|---|
| ndc | 55111-338-01 |
| ndc | 55111-338-05 |
| ndc | 55111-339-30 |
| ndc | 55111-339-01 |
| ndc | 55111-339-05 |
| ndc | 55111-340-30 |
| ndc | 55111-340-01 |
| ndc | 55111-340-05 |
| ndc | 55111-341-30 |
| ndc | 55111-341-01 |
| ndc | 55111-341-05 |
| code_info | C201293 Exp Date 08/2013 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1434-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.