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Acid Relief News (Page 2)
FDA Medwatch Alert: Sandoz Inc. Issues Voluntary Recall of Ranitidine Hydrochloride Capsules 150mg and 300mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA) in the Product
September 23, 2019 – Sandoz Inc. is voluntarily recalling all quantities and lots within expiry of Ranitidine Hydrochloride Capsules in the US to the consumer level because of confirmed...
FDA Medwatch Alert: Safety Information: Ranitidine Generics - NDMA Found in Samples of Some Ranitidine Medicines
September 13, 2019 ISSUE: FDA has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain a nitrosamine impurity called...
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