FDA Drug recall D-1144-2015
Amlodipine besylate and Atorvastatin calcium tablets, 10mg/10mg, packaged in a)30-count bottle (NDC 43598-321-30), b) 90-count bottle (NDC…
- FDA Drug
- Class III
- terminated
- Published 2015-06-24
On 2015-06-24 the FDA classified a Class III recall of Amlodipine besylate and Atorvastatin calcium tablets, 10mg/10mg, packaged in a)30-count bottle (NDC 43598-321-30), b) 90-count bottle (NDC… by Dr Reddy S Laboratories, citing subpotent drug.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1144-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-05-06 |
| Published | 2015-06-24 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Dr Reddy S Laboratories |
| Distribution | US |
Product
Amlodipine besylate and Atorvastatin calcium tablets, 10mg/10mg, packaged in a)30-count bottle (NDC 43598-321-30), b) 90-count bottle (NDC 43598-321-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India
Reason
Subpotent drug
Identifiers
| ndc | 43598-323-30 |
|---|---|
| ndc | 43598-323-60 |
| ndc | 43598-323-90 |
| ndc | 43598-323-05 |
| ndc | 43598-320-30 |
| ndc | 43598-320-60 |
| ndc | 43598-320-90 |
| ndc | 43598-320-05 |
| ndc | 43598-317-30 |
| ndc | 43598-317-60 |
| ndc | 43598-317-90 |
| ndc | 43598-317-05 |
| ndc | 43598-322-30 |
| ndc | 43598-322-60 |
| ndc | 43598-322-90 |
| ndc | 43598-322-05 |
| ndc | 43598-319-30 |
| ndc | 43598-319-60 |
| ndc | 43598-319-90 |
| ndc | 43598-319-05 |
| ndc | 43598-316-30 |
| ndc | 43598-316-60 |
| ndc | 43598-316-90 |
| ndc | 43598-316-05 |
| ndc | 43598-314-30 |
| ndc | 43598-314-60 |
| ndc | 43598-314-90 |
| ndc | 43598-314-05 |
| ndc | 43598-321-30 |
| ndc | 43598-321-60 |
| ndc | 43598-321-90 |
| ndc | 43598-321-05 |
| ndc | 43598-318-30 |
| ndc | 43598-318-60 |
| ndc | 43598-318-90 |
| ndc | 43598-318-05 |
| ndc | 43598-315-30 |
| ndc | 43598-315-60 |
| ndc | 43598-315-90 |
| ndc | 43598-315-05 |
| ndc | 43598-313-30 |
| ndc | 43598-313-60 |
| ndc | 43598-313-90 |
| ndc | 43598-313-05 |
| code_info | Lot #: a) C401537, Exp 07/2015; b) C401539, Exp 07/2015 |
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-1144-2015%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.