Reported Mar 25, 2020 · Terminated
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC
Perrigo Company PLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Perrigo Company PLC · 515 Eastern Ave · Allegan, MI · 49010-9070
Is this the product you have?
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC
13 of 13 products
| # | Product as published |
|---|---|
| 1 | Brand] NDC CVS Health: 69842-293-65 |
| 2 | NDC Equaline 41163-931-65 |
| 3 | NDC Family Wellness: 55319-876-65 |
| 4 | NDC Good Sense 0113-0876-65 |
| 5 | NDC H.E.B.: 37808-876-65 |
| 6 | NDC Harris Teeter: 69256-876-65 |
| 7 | NDC Health Mart: 62011-0283-1 |
| 8 | NDC Leader: 62011-0283-1 |
| 9 | NDC Major: 0904-6715-46 |
| 10 | NDC Signature Care: 21130-118-65 |
| 11 | NDC Sunmark: 49348-136-44 |
| 12 | NDC Up & Up: 11673-876-65 |
| 13 | NDC Walgreens: 0363-1876-65 |
- Lot codes and dates
- Lots
8DE13638EE15588FE14508GE13318HE12218KE28258JE19168KE22438ME26859AE27859AE27869DE27219CE33179EE25799FE29579GE27859GE32189HE3577
- Lots
This recall covers 17 products
The agency filed one notice per product. You are reading one of them; the other 16 are below.
4 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
This product could cause temporary or reversible health problems — stop using it.
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