This results in decreased gastric acid secretion and gastric volume, and reduced hydrogen ion concentration. A substance that could cause cancer has been found in the heartburn drug Zantac and several other antacids, the Food and Drug Administration announced Friday. Hours of operation are 9:00 am - 5:00 pm, EST Monday through Friday.Consumers who have Ranitidine Tablets, USP which are being recalled should stop using the product or with questions regarding this recall can contact Inmar Pharmaceuticals Services by 800-967-5952 (option 1). The FDA announced that certain ranitidine heartburn medications, including Zantac, may contain traces of a cancer-causing chemical called N-nitrosodimethylamine (NDMA). Ranitidine is a histamine-2 blocker, which decreases the amount of acid created by the stomach. Ranitidine Tablets 150 mg and 300 mg is a prescription oral product approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.Glenmark is committed to product and consumer safety. Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP), manufactured by Amneal, are prescription oral products. With the 2019 voluntary recall of ranitidine (brand name Zantac) and nizatidine (brand name Axid) products in the U.S. well underway due to contamination by the carcinogen NDMA, the FDA has listed several alternative drugs to treat heartburn and related conditions.. Proton Pump Inhibitors However, such contamination is considered unacceptable for a medicine. 'We are not children': Federal plan to increase arrivals cap infuriates WA PremierWoman flung through the air after garbage truck collects more than just the rubbishMan bitten by shark in fishing mishap off popular Queensland island Consumers, distributors and retailers that have Ranitidine Oral Solution, USP 150 mg/10 mL, which is being recalled, should stop using and call Precision Dose Inc. at 815-624-8523 to obtain a return packet.Consumers with questions regarding this recall can contact Precision Dose Inc. by phone (815-624-8523), Monday through Friday 8 am to 4:30 pm CST or e-mail us at: Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.GSMS, Inc. received a recall notification from the manufacturer, Novitium, on October 25th, 2019 and initiated a voluntary recall on November 6th, 2019 to the consumer level for 7 lots of Ranitidine HCl 150mg and 12 lots of Ranitidine HCl 300mg Capsules.To date, GSMS, Inc. has not received any reports of adverse events related to the use of the products as part of this recall.Ranitidine Hydrochloride Capsules are indicated for the treatment of duodenal ulcer, benign gastric ulcer, reflux esophagitis, post-operative peptic ulcer, Zollinger-Ellison Syndrome, and other conditions where reduction of gastric secretion and acid output is desirable.GSMS, Inc. has promptly notified its consignees via email and certified mail.
ZANTAC Injection Premixed solution, 50 mg, in 0.45% sodium chloride, 50 mL, requires no dilution and should be infused over 15 to 20 minutes. Following is a list of possible medication recalls, market withdrawals, alerts and warnings.
NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.Ranitidine is an over-the-counter (OTC) and prescription product indicated for the relief of heartburn associated with acid indigestion and sour stomach and prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages.After regulatory bodies announced that ranitidine may potentially contain NDMA, Perrigo promptly began testing of its externally sourced ranitidine API (active pharmaceutical ingredient) and ranitidine-based products. The Company is a leading provider of over-the-counter health and wellness solutions that enhance individual well-being by empowering consumers to proactively prevent or treat conditions that can be self-managed.
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