TOPIRAMATE

Riconpharma LLC received FDA approval for Topiramate (NDA 220041, strength 001).

Riconpharma LLC received FDA approval (NDA 220041, supplemental application 002) for a topiramate product.

Riconpharma LLC received FDA approval for topiramate (ANDA 220041, supplement 003), adding a new product record to the Orange Book.

RICONPHARMA LLC received FDA approval for TOPIRAMATE (topiramate) under NDA 220041, supplement 004.

Riconpharma LLC received FDA approval for Topiramate (ANDA 220041, supplement 005).