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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 ...
2d
Capital Market on MSNNatco Pharma receives USFDA EIR for Hyderabad API facility
In a regulatory filing made during market hours today, Natco Pharma announced that it has received an establishment ...
Q1FY26 revenues at ?12.7 billion, YoY growth of 142% and flat QoQ growth. This includes revenues from the acquired NRT business.
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