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Actavis South Atlantic Recalls
3 recalls on record · April 24, 2013 to September 4, 2013 · Drugs
September 4, 2013DrugsFDA
Actavis South Atlantic LLC recalls buPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, 30-count tablets per bottle, Rx only, Distributed by: Act
Hazard: Failed Dissolution Specifications: This recall is an extension of the recall initiated on 07/31/2013 for Bupropion HCl Extended-Release Tablets (XL) 300 mg, because another lot was shown to have similar failing results for dissolution at the 8-hour timepoint.
August 7, 2013DrugsFDA
Actavis South Atlantic LLC recalls Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL, Rx Only. Manufactured by VistaPharm, Inc., Birmingham, AL 352
Hazard: Failed Impurity/Degradation Specification; "Related Compound C"
April 24, 2013DrugsFDA
Actavis South Atlantic LLC recalls buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg, 30-count tablets per bottle, Rx only, Distributed by: Acta
Hazard: Failed USP Dissolution Test Requirements: Out-of-specification dissolution results at the 8 hour stability testing point.