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USFDA issues ‘DMF information request’ to SMS Pharmaceuticals

17 Sep 2019

US Food and Drug Administration (USFDA) has issued a ‘DMF information request’ to SMS Pharmaceuticals to provide the information to demonstrate its Ranitidine API manufacturing process does not contain NDMA impurity.

SMS Pharmaceuticals is a global player in API manufacturing having strong research and manufacturing team supported by state of art facilities.

Related SMS Pharmaceuticals Ltd. Links:

SMS Pharmaceuticals Share Price

131.00 1.80 (1.39%) Nov 26, 18:01
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