Jubilant Life receives US FDA approval for migraine drug zomitriptan

Jubilant Life Sciences Ltd, an integrated global pharmaceuticals and life sciences company, has received abbreviated new drug application (ANDA) final approval from the US Food and Drug Administration (US FDA) for zolmitriptan orally disintegrating tablets, 2.5 mg and 5 mg, the generic version of Zomig-ZMT (of Astra Zeneca), which is used for acute treatment of migraine headaches in adults.
 
As on June 30, 2015, Jubilant Life Sciences had a total of 815 filings for formulations of which 389 have been approved in various regions globally. This includes 72 ANDAs filed in the US, of which 38 have been approved and 46 dossier filings in Europe.