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[Update] The US FDA informed that Mylan announced the recall of three lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg. Mylan repackaged and distributed the affected lots that were manufactured by Qualitest Pharmaceuticals. They were distributed in unit dose (CD100) under the UDL Laboratories label. The affected lot numbers are: Lots 3037841, [...]

The US FDA informs Healthcare Professionals and Consumers that Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg are recalled because tablets may contain a higher dosage of acetaminophen that could lead to serious side effects. Background of Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg Hydrocodone bitartrate and acetaminophen 10 mg/500 mg tablets, [...]

Pharmacists and Consumers are informed by the FDA that Reese Pharmaceutical Company OTC Products are recalled because they were mislabeled as Guaifenesin tablets posing a threat of overdose to patients. Background of Reese Pharmaceutical Company OTC Products Refenesen Expectorant (guaifenesin 200 mg tablets), Select Brand Mucus Relief Expectorant (guaifenesin 200 mg), QC Medifin Expectorant (guaifenesin [...]

Healthcare personnel and consumers are informed by the FDA that Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg are recalled because there is a potential of higher dosage of acetaminophen that could result in liver toxicity. Background of Qualitest Hydrocodone Bitartrate and Acetaminophen Tablets 10 mg/500 mg Hydrocodone bitartrate and acetaminophen 10 mg/500 mg [...]