FDA Drug recall D-1317-2020
Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, I…
- FDA Drug
- Class II
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, I… by Torrent Pharma, citing failed Dissolution Specifications.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1317-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-05-11 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Torrent Pharma |
| Distribution | US |
Product
Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals Ltd, Bharuch 392130, India; Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920, NDC 13668-268-05
Reason
Failed Dissolution Specifications
Identifiers
| ndc | 13668-268-30 |
|---|---|
| ndc | 13668-268-01 |
| ndc | 13668-268-10 |
| ndc | 13668-268-31 |
| ndc | 13668-268-05 |
| ndc | 13668-271-01 |
| ndc | 13668-271-10 |
| ndc | 13668-271-49 |
| ndc | 13668-271-05 |
| code_info | Lot #: 4FF4F001, Exp 1/2023 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1317-2020%22
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