FDA Drug recall D-0315-2020
Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Tablets NDC 0363-1029-03 Distributed By: Walgreen Co.,…
- FDA Drug
- Class II
- completed
- Published 2019-11-20
On 2019-11-20 the FDA classified a Class II recall of Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Tablets NDC 0363-1029-03 Distributed By: Walgreen Co.,… by Apotex, citing GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0315-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-09-24 |
| Published | 2019-11-20 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Apotex |
| Distribution | US |
Product
Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Tablets NDC 0363-1029-03 Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015
Reason
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
Identifiers
| code_info | All lots remaining within expiry. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.
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FDA Drug · Class II · 2025-10-08 · Apotex
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0315-2020%22
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