Eugia Pharma receives USFDA approval for Bortezomib
Drug Approval

Eugia Pharma receives USFDA approval for Bortezomib

The approved product has a market size of US $ 1172 million for the twelve months ending March 2022, according to IQVIA

  • By IPP Bureau | May 04, 2022

Aurobindo Pharma’s wholly owned subsidiary company, Eugia Pharma Specialties has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Bortezomib for injection, 3.5 mg. Bortezomib for Injection, 3.5 mg/vial (Single-Dose Vial) to be bioequivalent and therapeutically equivalent to the Velcade for Injection 3.5 mg/vial, of Takeda Pharmaceuticals U.S.A. The product is being launched immediately. The approved product has a market size of US $ 1172 million for the twelve months ending March 2022, according to IQVIA.

This is the 136th ANDA (including 7 tentative approvals) to be out of Eugia Pharma Specialty Group (EPSG) facilities, manufacturing both oral and sterile specialty products.

 

 

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