Eli Lilly Gets CDSCO Panel Nod for Ixekizumab Safety Label Update
Written By : Dr. Divya Colin
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2025-08-09 07:00 GMT | Update On 2025-08-09 07:00 GMT
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New Delhi: Eli Lilly and Company (India) Pvt Ltd has secured regulatory clearance from the Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) for updating the package insert of its drug Ixekizumab Solution for Injection 80 mg/mL, in both pre-filled autoinjector and pre-filled syringe formats.
The approval pertains to Package Insert Version 2 dated November 2024, incorporating changes in the sections of Special Warnings and Precautions for Use, Undesirable Effects, Post-Marketing Experience, and Patient Counselling Information. These updates are aligned with the USFDA package insert update approval dated 20th August 2024.
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