Reported Jan 15, 2020 · Ongoing
Glenmark Ranitidine Tablets USP 150 mg Rx Only 500 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd.…
Glenmark Pharmaceuticals Inc., USA
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: Glenmark Pharmaceuticals Inc., USA · 750 Corporate Dr · Mahwah, NJ · 07430-2009
Is this the product you have?
- Glenmark Ranitidine Tablets USP 150
- mg Rx Only 500 Tablets Manufactured byGlenmark Pharmaceuticals Ltd. Colvale-Bandez, Goa 403513
- India Manufactured forGlenmark Pharmaceuticals Inc., USA Mahwah, NJ NDC 68462-248-05
- Lot codes and dates
616 of 616 codes
7701034A7701057A7701058A7701059A7701060A7701061A7701071A7701072A7701073A7701074A7701105A7701106A7701107A7701108A7701109A7701113A7701114A7701115A7701116A7701121A7701122A7701123A7701124A7701125A7701126A7701151A7701152A7701165A7701154A7701155A7701163A7701176A7701190A7701221A7701222A7701223A7701224A7701225A7701235A7701253A7701254A7701255A7701256A7701257A7701258A7701259A7701266A7701267A7701268A7701273A7701275A7701276A7701277A7701294A7701295A7701296A7701297A7701300A7701301A7701302A
- Amount recalled
- 1,712,632 bottles
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Why it was recalled
CGMP Deviations: Presence of NDMA impurity detected in product.
This product could cause temporary or reversible health problems — stop using it.
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