Reported May 11, 2022 · Terminated
Losartan Potassium Tablets USP, 25 mg, a) 90-count bottles (NDC# 68180-376-03), b) 1000-count bottles (NDC#…
Lupin Pharmaceuticals Inc.
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: Lupin Pharmaceuticals Inc. · Harborplace Tower · Baltimore, MD · 21202-6174
Is this the product you have?
Losartan Potassium Tablets USP25 mga) 90-count bottles (NDC# 68180-376-03)b) 1000-count bottles (NDC# 68180-376-09)Rx Only
- Manufactured ByLupin Limited, Pithampur, India
- MFG ForLupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, USA
- Lot codes and dates
H001333exp. date Nov-22 H002786exp. date Jan-23 H101282exp. date Feb-23 H001189exp. date Nov-22 H002955exp. date Jan-23 H101285exp. date Feb-23 H001714exp. date Dec-22 H000523exp. date Jan-23 H101989exp. date Mar-23 H001940exp. date Dec-22 H003080exp. date Jan-23 H101789exp. date Mar-23 H002388exp. date Jan-23 H100109exp. date Feb-23 H002389exp. date Jan-23 H100642exp. date Feb-23 H000848exp. date Nov-22H002002exp. date Dec-22 H100110exp. date Feb-23 H001190exp. date Nov-22 H002003exp. date Dec-22 H100111exp. date Feb-23 H001191exp. date Nov-22 H002489exp. date Jan-23 H100146exp. date Feb-23 H001192exp. date Nov-22 H002390exp. date Jan-23 H100147exp. date Feb-23 H001058exp. date Nov-22 H002486exp. date Jan-23 H101283exp. date Feb-23 H000985exp. date Nov-22 H002487exp. date Jan-23 H101284exp. date Feb-23 H001059exp. date Nov-22 H002488exp. date Jan-23 H100643exp. date Feb-23 H001275exp. date Nov-22 H002787exp. date Jan-23 H100644exp. date Mar-23 H001715exp. date Dec-22 H002957exp. date Jan-23 H100869exp. date Mar-23 H001716exp. date Dec-22 H002958exp. date Jan-23 H101990exp. date Mar-23 H001717exp. date Dec-22 H003079exp. date Jan-23 H101991exp. date Mar-23 H001718exp. date Dec-22 H003121exp. date Feb-23 H101992exp. date Mar-23 H001941exp. date Dec-22 H003122exp. date Feb-23 H000847exp. date Nov 2022
- Amount recalled
- 657,336 bottles
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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