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ranitidine

Aurobindo recalls prescription and over-the-counter ranitidine

14 November 2019 | By Rachael Harper (European Pharmaceutical Review)

Aurobindo has recalled prescription and over-the-counter ranitidine due to the medications containing unacceptable levels of NDMA.

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FDA releases statement on ranitidine testing results

7 November 2019 | By Victoria Rees (European Pharmaceutical Review)

The FDA has issued a statement on the results from ranitidine medication testing for nitrosamines, saying that they contain no more NDMA than smoked meats.

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MHRA announces recall of Perrigo ranitidine products

28 October 2019 | By Victoria Rees (European Pharmaceutical Review)

The UK healthcare agency has issued an alert for Perrigo ranitidine products, recalling and quarantining certain batches.

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Sandoz voluntarily recalls ranitidine over NDMA contamination concerns

26 September 2019 | By Nikki Withers (European Pharmaceutical Review)

The probable carcinogen N-nitrosodimethylamine was detected in Sandoz’s ranitidine capsules, prompting the voluntary move.

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EMA to provide guidance on avoiding nitrosamines in medicines

17 September 2019 | By Victoria Rees (European Pharmaceutical Review)

The EMA has announced it is drafting guidance on how to avoid the presence of nitrosamines, a probable carcinogenic ingredient, in drugs.

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Recommended

ranitidine

Aurobindo recalls prescription and over-the-counter ranitidine

FDA releases statement on ranitidine testing results

MHRA announces recall of Perrigo ranitidine products

Sandoz voluntarily recalls ranitidine over NDMA contamination concerns

EMA to provide guidance on avoiding nitrosamines in medicines