Glenmark Pharmaceutical recalls ranitidine tablets in US
The tablets are being recalled because of the presence or potential presence of N-nitrosodimethylamine (NDMA) levels above the…
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NDMA
Glenmark recalls over two lakh cartons of product in US
According to the latest Enforcement Report by the US Food and Drug Administration (USFDA), Glenmark Pharmaceuticals Inc USA is…
Strides announces relaunch of ranitidine tablets for the US Market
Product to be relaunched with immediate effect
After sartans and ranitidine, where will NDMA show up next?
While regulators and pharma companies try to understand if it is the product or the process that is at fault in the ranitidine…
Dr Reddy’s recalls all its ranitidine products in US
The recall started on October 1 after USFDA found the presence of NDMA in certain ranitidine products above the permissable levels…
FDA says new test finds “unacceptable levels” of impurity in heartburn drugs
However, the agency said its testing method found much lower levels of the impurity, N-nitrosodimethylamine (NDMA), than a higher…
Dr Reddy’s halts worldwide supply of ranitidine
USFDA probing into the reported impurity N-nitrosodimethylamine in it at low levels