Correction to my previous post in this thread: LLY may decide to sue EGRX when the FDA accepts EGRX's RTU-Alimta NDA for review and EGRX notifies LLY of a Paragraph-IV challenge (not when the FDA approves the product for marketing).
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”