Tuesday, September 15, 2009

US FDA accepts for filing Mylan's ANDA for generic Copaxone

Mylan Inc. announced that the US Food and Drug Administration (FDA) has accepted for filing Mylan Pharmaceutical Inc.'s abbreviated new drug application (ANDA) for glatiramer acetate injection (20 mg/mL), a generic version of Teva's Copaxone, a product indicated for the treatment of multiple sclerosis.


The details can be read here.

No comments: