The United States Food and Drug Administration (USFDA) issued Form 483 with two observations after an inspection at Dr. Reddy’s Laboratories FTO 11 formulation manufacturing plant in Srikakulam, Andhra Pradesh.
The pharmaceutical major said it would respond to submissions within the timeframe. The pre-approval inspection (PAI) took place from June 30, 2022 to July 7, 2022.
Dr. Reddy’s laboratories are engaged in the supply of medicines. The Company operates in three segments: Global Generics, Pharmaceutical Services and Active Ingredients (PSAI) and Proprietary Products.
The big pharma’s consolidated net profit fell by 82.6% to Rs 97 crore on a 15% rise in operating income to Rs 5,436.80 crore in Q4 FY22 from Q4 FY21.
Shares of Dr Reddy Laboratories fell 0.03% to Rs 4,337.25 on BSE.
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(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)
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