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| Ranitidine |
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Formulary
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For use in patients with swallowing difficulties or via nasogastric tubes only |
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| Ranitidine |
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Formulary
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The European Medicines Agency (EMA) Human Medicines Committee (CHMP) has recommended the suspension of all ranitidine medicines due to the presence of low levels of the impurity N-nitrosodimethylamine (NDMA). (30 April 2020)
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| Ranitidine |
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Formulary
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