FDA Drug recall D-0182-2020
Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-34 (OTC)
- FDA Drug
- Class II
- completed
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-34 (OTC) by Dr Reddy S Laboratories, citing CGMP Deviations: Presence of NDMA impurity detected in product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0182-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-10-01 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Dr Reddy S Laboratories |
| Distribution | US |
Product
Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-34 (OTC)
Reason
CGMP Deviations: Presence of NDMA impurity detected in product.
Identifiers
| ndc | 55111-404-34 |
|---|---|
| ndc | 55111-404-32 |
| ndc | 55111-404-36 |
| ndc | 55111-404-50 |
| ndc | 55111-404-61 |
| ndc | 55111-404-55 |
| ndc | 55111-404-62 |
| ndc | 55111-404-90 |
| ndc | 55111-404-02 |
| ndc | 55111-404-65 |
| ndc | 55111-404-17 |
| ndc | 55111-404-24 |
| ndc | 55111-404-38 |
| ndc | 55111-404-40 |
| code_info | Batch Numbers: All lots within expiry. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0182-2020%22
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