Guest guest Posted December 14, 2010 Report Share Posted December 14, 2010 Natco first to file with USFDA for generic lenalidomide partnering with Pharmaceuticals Inc., USA. Natco has filed an Abbreviated New Drug Application (ANDA) with the U.S. Food and Drug Administration (FDA) seeking approval to market its LENALIDOMIDE 5, 10, 15 and 25 mg products strengths. Natco's LENALIDOMIDE tablets are generic versions of Celgene's Revlimid® Tablets. Upon successful commercialization, and Natco will share net profits on sales. will assume responsibility for ongoing regulatory, legal, and commercial expenses related to Natco's LENALIDOMIDE product. Source:http://www.natcopharma.co.in/usfda.html Celgene filed the lawsuit on October 8, 2010 in the United States District Court for the District of New Jersey seeking to prevent NATCO from commercializing its product prior to the expiration of certain U.S. Patents. http://www.natcopharma.co.in/celgene_sues_natco.html ~chris CLL CANADA Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.