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Total 5 results found. Search for [ Dr Reddy's Duvvada facility in Andhra Pradesh ]

Results 1 to 5 of 5
New Delhi, February 16, 2020
As notified by the USFDA, the inspection classification of Dr Reddy's Duvvada facility has been determined as 'Voluntary Action Initiated'

E Kumar Sharma
January 28, 2020
According to analysts, the company posted \"a good set of numbers, especially from the point of margin performance\" for the third quarter. As for the USFDA inspection, the current inspection gains importance given that it is last of the pending warning letters awaiting clearance

February 16, 2019

E Kumar Sharma
November 6, 2015
The action follows the earlier inspections of these sites by the agency.

BT Online
New Delhi, November 6, 2015
The stock fell after the drug major received a warning letter from US FDA on their API manufacturing facilities at Srikakulam and Oncology formulation facility at Duvvada in Andhra Pradesh.