greenstone alprazolam recall lotrisone

Expiration date is September 2020.Consumers that have been prescribed the recalled medication should contact Stericycle at 1-888-843-0255 for a documentation packet to return the drug. A health expert urged all sexually active women in Northern Ireland to take folic acid supplements to reduce the occurrence of serious birth defects. Greenstone has notified wholesalers/retailers to arrange for return of any recalled product.Distributors or retailers with an existing inventory of the lots, which are being recalled, should stop use and distribution and quarantine immediately. Diphenoxylate hydrochloride and atropine sulfate tablets are contraindicated in pediatric patients less than 6 years of age due to the risks of respiratory and central nervous system (CNS) depression.The use of this product in patients with uncontrolled diarrhea due to chronic medical conditions may predispose the patient to toxicity from either the diphenoxylate or atropine components. For retailers that have dispensed product to consumer customers, please notify these customers regarding the recall. The use of the impacted super potent product when used as labeled has a low probability of being associated with adverse events of limited severity such as lethargy, skin flush, and drowsiness. The recall involves alprazolam tablets, USP C-IV, 0.5 mg in 500-count bottles, lot No. The NDC number on the bottle is 0378-4003-05, and the lot number is 8082708. The product label states that over dosage can be life-threatening and symptoms may include opioid and/or anticholinergic effects including respiratory depression, coma, delirium, lethargy, dryness of the skin and mucous membranes, mydriasis or miosis, flushing, hyperthermia, tachycardia, hypotonia, tachypnea, toxic encephalopathy, seizures and incoherent speech. Alprazolam is used for the management of anxiety and panic disorders. The affected diphenoxylate hydrochloride and atropine sulfate lots include the following lot numbers and expiration dates. To date, there have been no reports of adverse events related to this recall.Diphenoxylate hydrochloride and atropine sulfate tablets are packaged in bottles of 100-count (NDC 59762-1061-1) and 1000-count (NDC 59762- 1061-2). Drug manufacturer, Mylan Pharmaceuticals Inc., issued a voluntary nationwide recall of one lot of Alprazolam tablets because of the presence of a foreign substance. The affected medication was distributed in the U.S. from July 2019 to August 2019. FDA does not endorse either the product or the company.For Immediate Release – PEAPACK, NJ, November 16, 2017 - Greenstone LLC, a wholly owned subsidiary of Pfizer Inc., is  voluntarily recalling multiple lots of diphenoxylate hydrochloride and atropine sulfate tablets, USP to the consumer level. Greenstone initiated this recall because product from these lots has the potential to be super potent or sub potent.Diphenoxylate hydrochloride and atropine sulfate tablets are indicated as adjunctive therapy in the management of diarrhea in patients 13 years of age and older. According to Mylan, “impact from the foreign material is expected to be rare but remote risk of infection cannot be ruled out.”Shares of Mylan stock were up 0.48 percent as of 9:31 a.m. The recall affects one lot of the drug that is packaged in 500 count bottles in a 0.5 mg dosage. For additional assistance, call Stericycle at 1-855-215-4982 between the hours of 8 a.m. to 5 p.m. Respiratory depression has been reported up to 30 hours after ingestion and may recur despite an initial response to narcotic antagonists. The anxiety medication Alprazolam, also known as Xanax, is being recalled by The recall affects one lot of the drug that is packaged in 500 count bottles in a 0.5 mg dosage. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. The lot was distributed in July and August. Medications listed here may also be marketed under different names in different countries. ET or by email at Consumers that have experienced problems from the recalled medication should contact their healthcare provider.The company has not received any reports of adverse reactions due to the recalled medication. Questions about the recall can be directed to Mylan Customer Relations by calling 1-800-796-9526, Monday through Friday from 8 a.m. to 5 p.m. 8082708, with a September 2020 expiration date. Due to Possible Sub Potent and Super Potent Tabletsdiphenoxylate hydrochloride and atropine sulfate tablets, USPAn official website of the United States government: Greenstone initiated this recall because product from these lots has the potential to be super potent or sub potent. If a patient was to receive a sub potent tablet, symptoms may not be controlled. Recalls, Market Withdrawals, & Safety Alerts If you take a generic version of Xanax for anxiety you should check your medication against a new recall. ET on Monday. If you have further distributed the recalled product, to the wholesale or retail level, please notify any accounts or additional locations which may have received the recalled product from you. Products were distributed nationwide to wholesalers/retailers from November 2016 through June 2017 in the United States.Pfizer  places  the  utmost  emphasis  on  patient  safety and product quality at every step in the manufacturing and supply chain process.Patient safety is our first priority.

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