CDSCO Panel Approves Updated Package Insert for Takeda's Vedolizumab
Written By : Susmita Roy
Published On 2025-11-05 10:46 GMT | Update On 2025-11-05 10:46 GMT
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New Delhi: In a key regulatory development, the Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has approved the updated package insert for Vedolizumab 300 mg and 108 mg powder for concentrate for solution for infusion, marketed by Takeda Biopharmaceuticals India.
The company had presented its proposal seeking approval for amendments in Section 4.6 (Use in Special Population) of the drug’s package insert, aligning it with the Company Core Data Sheet (CCDS) Version 9.0
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