fda
1 records
FDA Drug Recall: Quinacrine Dihydrochloride (98.25%), bulk API product, packaged in a) 500 g NDC#
2019-10-02
Class I — Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.
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ny_corps
1 records
NY Corp: DARMERICA, LLC
2025-06-06
FOREIGN LIMITED LIABILITY COMPANY | County: Albany | Jurisdiction: Florida
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