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The U.S. FDA had inspected the API facility, in Mekaguda here, from June 9-13 and issued Form 483 with one observation. The regulator had classified it as “voluntary action indicated” (VAI), the ...
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Capital Market on MSNNatco Pharma receives USFDA EIR for Hyderabad API facility
Natco Pharma shares slipped 2.5% to Rs 1,009 apiece on the BSE in Thursday’s trade after the company announced its plan to ...
Q1FY26 revenues at ?12.7 billion, YoY growth of 142% and flat QoQ growth. This includes revenues from the acquired NRT business.
A Form 483 is issued by the US health regulator when inspectors identify conditions that may violate the Food, Drug, and ...
A Form 483 is issued at the conclusion of an inspection when USFDA investigators observe conditions that may be in violation ...
Dr Reddy’s received a Form 483 with seven USFDA observations after inspecting its Srikakulam manufacturing plant in Andhra ...
Dr Reddy's Laboratories has received a Form 483 with seven observations from the US health regulator for its Srikakulam-based ...
Dr. Reddy's Laboratories receives a Form 483 with seven observations from the USFDA after an inspection of its Srikakulam ...
Dr Reddy's Laboratories received a Form 483 with seven observations from the USFDA for its Srikakulam-based plant in Andhra ...
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