New Delhi: Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (USFDA) for Eltrombopag Tablets, 12.5 mg, 25 mg, 50 mg, and 75 mg (USRLD: Promacta Tablets, 12.5 mg, 25 mg, 50 mg, and 75 mg).Eltrombopag tablets are indicated for the treatment of thrombocytopenia (low platelet count) in specific blood disorders. The drug works by stimulating bone marrow cells to produce more platelets, thereby reducing the risk of bleeding.Also Read: Zydus-Owned Sentynl Gets USFDA Nod for First-Ever Menkes Disease Treatment ZYCUBOEltrombopag tablets will be produced at the group’s formulation manufacturing facility at SEZ, Ahmedabad. Eltrombopag tablets had annual sales of USD 1,262.5 million in the United States (IQVIA MAT Nov-2025).The group now has 429 approvals and has so far filed 505* ANDAs since the commencement of the filing process in FY 2003–04.Also Read: Gujarat HC Halts DGGI Action on Rs 56.33 Cr GST Demand Against Zydus Unit