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Zydus Lifesciences gets USFDA EIR for API Ahmedabad facility
Ahmedabad: Zydus Lifesciences has announced that the Company has received the EIR report from the United States Food and Drug Administration (USFDA) for the inspection conducted at the API Ahmedabad facility.
The company had earlier received Post Application Action Letter from the USFDA for the same inspection confirming that the inspected facility has been considered as ready to commercially manufacture and supply the API.
Read also: USFDA gives nod for commercial production at Zydus Ahmedabad API unit
"This facility underwent an inspection from 14th to 22nd Dec 2023 and has been classified as Voluntary Action Indicated (VAI)," the Company stated in a BSE filing.
Formerly known as Cadila Healthcare Limited, Zydus Lifesciences Limited is an Indian multinational pharmaceutical company headquartered in Ahmedabad. The company is primarily engaged in the production of generic drugs. Cadila was founded in 1952 by Ramanbhai Patel.
Read also: Zydus Lifesciences aims to launch first new drug in US by early 2026
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751
Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751