Darmerica, LLC Recalls

FDA
1
Total Recalls
1
Agencies
Oct 2019
First Recall
Oct 2019
Latest Recall

Showing 1-1 of 1 recalls

FDA

Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC# 71052-530-05; b) 50 g NDC# 71052-530-55, c) 25g NDC# 71052-530-25, Darmerica LLC 198 Wilshire Blvd Casselberry, FL 32707

Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.