That's the point. They'd be nuts to continue to charge blindly into windmills with the same old Lupenox. What they are presenting now must be an altered product. Otherwise they're incompetent boobs. ...
The theory being tossed is that the product has been altered, but is still Lupenox because ItaliaPh has changed the process for all.
So, 2006 Lupenox hits the market and is the exact same drug in TEVA's ANDA. Sometime after that TEVA has IP alter the product based on what the FDA is saying. Nobody in India would care, so that would be invisible there w/o outside testing.
This makes everybody correct.
DD] mL IS Lupenox RR] The 2006 Lupenox had no chance with the FDA