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20 April 2020 | By Victoria Rees (European Pharmaceutical Review)
The FDA has said that Amneal Pharmaceuticals is recalling three lots of nizatidine oral solution at the consumer level due to potential NDMA contamination.
28 February 2020 | By Hannah Balfour (European Pharmaceutical Review)
Ranitidine tablets have been recalled due to the possibility of the products containing unacceptable levels of NDMA.
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