🧬 Interested in pharma, biotech and medical device news? Visit PharmaDeviceNews.com →

Zydus Lifesciences gets FDA approval for Bortezomib for Injection

Zydus Lifesciences (previously called Cadila Healthcare) said that it has secured final approval from the US Food and Drug Administration (FDA) to market Bortezomib for Injection, 3.5 mg/vial, Single-Dose Vial.

Bortezomib for Injection is the generic of Velcade (bortezomib), which has a market size of $1.17bn as per IQVIA MAT March 2022.

It is used for the treatment of some forms of cancer that include multiple myeloma and mantle cell lymphoma.

The drug works by either slowing or stopping the growth of cancer cells.

Zydus Lifesciences gets FDA approval for Bortezomib for Injection
Zydus Lifesciences gets FDA approval for Bortezomib for Injection. Photo courtesy of Zydus Cadila.

Bortezomib for Injection will be manufactured at Zydus Hospira.

Zydus Lifesciences currently has 331 approvals and till now has submitted more than 400 abbreviated new drug applications (ANDAs) since the start of filing process in FY 2003-04.


Discover more from Business-News-Today.com

Subscribe to get the latest posts sent to your email.

Total
0
Shares
Related Posts
Read More

ALTA-1L trial results : Takeda’s ALUNBRIG continues to show superiority over crizotinib

ALTA-1L trial results : Takeda Pharmaceutical says that ALUNBRIG (brigatinib), its tyrosine kinase inhibitor (TKI), is continuing to show superiority over crizotinib in the phase 3 ALTA-1L trial. The Japanese pharma company released updated data from the late-stage trial involving adult patients having advanced anaplastic lymphoma kinase-positive (ALK+) non-small cell lung cancer (NSCLC) who did […]