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Tag: Dr. Reddy’s

Dr. Reddy’s Q1 net plunges 69% to ₹435.6 cr on lower revenue

Posted on July 22, 2026 By admin
Dr. Reddy’s Q1 net plunges 69% to ₹435.6 cr on lower revenue

Hyderabad-based generic drugmaker Dr. Reddy’s Laboratories’ consolidated net profit slumped 69% year-on-year (YoY) to ₹.435.6 crore in the June quarter amid lower sales of cancer drug lenalidomide and nearly ₹240 crore provision necessitated by recent quality issue around weight loss drug Semaglutide. Total revenue from operations stood at ₹8,099.8 crore (₹8,572.1 crore), showed its results…

Read More “Dr. Reddy’s Q1 net plunges 69% to ₹435.6 cr on lower revenue” »

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Dr. Reddy’s Q4 dips 86% on lower sales, multiple one offs to ₹221 crore

Posted on May 13, 2026 By admin
Dr. Reddy’s Q4 dips 86% on lower sales, multiple one offs to ₹221 crore

On the SSA, the company said it recorded ₹453 crore as a reduction of revenue from sale of goods in its Global Generics Segment. | Photo Credit: The Hindu Pharma major Dr. Reddy’s Laboratories reported consolidated net profit slumped to ₹221.3 crore for the March quarter compared to ₹1,586.7 crore a year earlier on the…

Read More “Dr. Reddy’s Q4 dips 86% on lower sales, multiple one offs to ₹221 crore” »

Business

Dr. Reddy’s gets inspection report from USFDA for Srikakulam-based API plant

Posted on September 6, 2024 By admin
Dr. Reddy’s gets inspection report from USFDA for Srikakulam-based API plant

Dr. Reddy’s Laboratories on Friday (September 6, 2024) said it has received the establishment inspection report (EIR) from the U.S. health regulator for its active pharmaceutical ingredient manufacturing facility (CTO-6) in Srikakulam, Andhra Pradesh. The U.S. Food and Drug Administration (USFDA) has classified the inspection as Voluntary Action Indicated (VAI) and concluded that the inspection…

Read More “Dr. Reddy’s gets inspection report from USFDA for Srikakulam-based API plant” »

Business

Dr. Reddy’s biosimilar of Roche’s cancer drug gets EMA panel nod

Posted on July 29, 2024 By admin
Dr. Reddy’s biosimilar of Roche’s cancer drug gets EMA panel nod

Dr. Reddy’s had previously received EU (Good manufacturing practice) GMP certificate for its Rituximab drug substance and drug product manufacturing facility located in Hyderabad.  The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending launch of Dr. Reddy’s Laboratories’ proposed biosimilar Rituximab candidate DRL_RI…

Read More “Dr. Reddy’s biosimilar of Roche’s cancer drug gets EMA panel nod” »

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