BDR Pharmaceutical Gets CDSCO Panel Nod for Bioequivalence Study of Elobixibat tablet
Written By : Dr. Divya Colin
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2025-01-01 12:15 GMT | Update On 2025-01-01 12:15 GMT
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New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has granted approval to the drug maker BDR Pharmaceutical to conduct a bio-equivalence study of Elobixibat Tablets 5 mg.
Furthermore, the expert panel stated that the result of the bio-equivalence study should be presented before the committee for further consideration.
This came after BDR Pharmaceutical presented the proposal for grant of permission to manufacture and market Elobixibat Tablets 5 mg along with the bioequivalence study protocol before the committee.
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