Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 60 tablets per bottle. [NDC: Brand] NDC Health Mart: 62011-0283-2; NDC Major: 0904-6715-52; NDC Meijer: 41250-252-72; NDC Sunmark: 49348-136-12;
Reported: March 25, 2020 Initiated: October 23, 2019 #D-1013-2020
Product Description
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 60 tablets per bottle. [NDC: Brand] NDC Health Mart: 62011-0283-2; NDC Major: 0904-6715-52; NDC Meijer: 41250-252-72; NDC Sunmark: 49348-136-12;
Reason for Recall
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Details
- Recalling Firm
- Perrigo Company PLC
- Distribution
- Nationwide USA
- Location
- Allegan, MI
Frequently Asked Questions
What product was recalled? ▼
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 60 tablets per bottle. [NDC: Brand] NDC Health Mart: 62011-0283-2; NDC Major: 0904-6715-52; NDC Meijer: 41250-252-72; NDC Sunmark: 49348-136-12;. Recalled by Perrigo Company PLC.
Why was this product recalled? ▼
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 25, 2020. Severity: Moderate. Recall number: D-1013-2020.
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