FDASeptember 6, 2019drug
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
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
What to do
FDA enforcement status: Terminated
Brands named
darmerica
Recall history
No related federal recalls on record for this brand yet.
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