Glenmark Pharmaceuticals Inc., USA: Glenmark Ranitidine Tablets USP 150 mg
Recall reason: CGMP Deviations: Presence of NDMA impurity detected in product.. Recalled by Glenmark Pharmaceuticals Inc., USA. Distribution: Natiowide. Classification (Class II — potential health risk). Affected lots/NDC/dates: 7701033A 7701826A 7702344A 7702345A 7702489A 7702706A 7702707A 7702708A 7702858A 7702859A 7702860A 7702928A. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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