";s:4:"text";s:4445:" Mylan Pharmaceuticals Inc. has recalled a single lot of Verapamil HCI Extended-release capsules, 180 mg. The FDA Alert(s) below may be specifically about amphetamine/dextroamphetamine or relate to a group or class of drugs which include amphetamine/dextroamphetamine.MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. FDA and the Agency for Healthcare Research and Quality are sponsoring a large epidemiological study that will provide further information about the potential risks associated with stimulant medication use in children. Available Products. Manufacturer Teva has issued a voluntary recall of two lots of generic Adderall, also known as amphetamine salts or amphetamine salt combo.. A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market.The list below includes voluntary recalls in which public notification has been issued. Sun Pharma discontinued amphetamine mixed salts in 2019. ... Mylan did not provide a reason for the shortage; Teva has brand name Adderall and generic amphetamine mixed salts available. Verapamil HCl Extended-Release Tablets Status: Discontinuation »Therapeutic Categories: Cardiovascular. Select one or more newsletters to continue. Mallinckrodt has amphetamine mixed salts available. Uses. Available for Android and iOS devices. A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market. A drug recall is the most effective way to protect the public from a defective or potentially harmful product. May 30, 2012. An official website of the United States government Following is a list of possible medication recalls, market withdrawals, alerts and warnings. The product is being recalled because the affected lot may contain some tablets exceeding weight requirements which may lead to super-potent tablets.Clinically significant adverse reactions to a supratherapeutic dose could include cardiovascular, neurologic, psychiatric and gastrointestinal reactions. Lot number 3018380 has been recalled because this lot failed the manufacturer routine tests that measure the capsules' ability to dissolve.