Hours of operation are 9:00 am - 5:00 pm, Eastern Standard Time (EST) Monday thru Friday.Any general questions regarding the return of this product please contact Inmar Pharmaceuticals Services at 800-967-5952 (option 1). How to use Ranitidine Hcl Tablet Peptic Ulcer Agents. Copy the URL below and paste it into your RSS Reader application.

Bridgewater, New Jersey is voluntarily recalling Ranitidine Tablets, USP, 150 mg and 300 mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, are being recalled because of potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.Amneal Pharmaceuticals, LLC. Each tablet, for oral administration contains 168 mg or 336 mg of ranitidine hydrochloride equivalent to 150 mg and 300 mg of ranitidine, respectively. Patients should contact their healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

This recall is being initiated in response to the recall by the manufacturer (Lannett Company, Inc.), which included affected lots that were repackaged by American Health Packaging.NDMA is classified as a probable human carcinogen, a substance that can cause cancer, based on laboratory testing. As a further precautionary measure, Glenmark ceased distribution of its Ranitidine products in the United States while it continues its efforts to test and investigate in cooperation with the FDA.To date, Glenmark has not received any reports of adverse events that have been confirmed to be directly related to this recall. Copy the URL below and paste it into your RSS Reader application.DailyMed will deliver notification of updates and additions to Drug Label information currently shown on this site through its RSS feed.DailyMed will deliver this notification to your desktop, Web browser, or e-mail depending on the RSS Reader you select to use. Ranitidine is a histamine-2 blocker, which decreases the amount of acid created by the stomach. Once an alternative treatment has been prescribed, the patients are instructed to contact Novitium‘s recall processor to obtain instructions and kit for returning the remaining product in their possession.Consumers with questions regarding this recall can contact GSMS, Inc, by: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.November 12, 2019 -- Amneal Pharmaceuticals, LLC. Ranitidine Tablets, USP and Ranitidine Syrup (Ranitidine Oral Solution, USP), manufactured by Amneal, are prescription oral products. Ranitidine Hydrochloride is a member of the class of histamine H2-receptor antagonists with antacid activity. OTC Ranitidine Tablets are also used to prevent heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages. No reports of injury or adverse events to date.Ranitidine is used as a short-term treatment for active duodenal ulcers, maintenance therapy for duodenal ulcer patients, treatment of pathological hypersecretory conditions, short-term treatment of active, benign gastric ulcers, maintenance therapy for gastric ulcers, treatment of GERD and treatment of endoscopically diagnosed erosive esophagitis.Product was distributed Nationwide to Wholesalers for use in hospital settings.American Health Packaging has notified its distributors by recall letter, sent November 1st, 2019, to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts. Ranitidine has been used to treat and prevent ulcers in the stomach and intestines. 57896-713-03, Erosive Esophagitis Patient Healing Rates Carcinogenesis, Mutagenesis, Impairment of Fertility:Pathological Hypersecretory Conditions (such as Zollinger-Ellison syndrome):Maintenance of Healing of Duodenal and Gastric Ulcers: Dosage Adjustment for Patients With Impaired Renal Function: Store between 20° and 25°C (68°and 77°F) in a dry place. Consumers are asked to continue taking their medication and speak to their physician or pharmacist on alternate healthcare treatment options.Consumers with questions regarding this recall can contact Sandoz at 1-800-525-8747 option # between 8:30am – 5:00pm Monday – Friday EST or 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 AdministrationHealthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:Gavreto (pralsetinib) is an oral selective RET kinase inhibitor for the...Detectnet (copper Cu 64 dotatate) is a radioactive diagnostic agent indicated...Onureg (azacitidine) is a nucleoside metabolic inhibitor indicated for the...Qdolo (tramadol hydrochloride) is an opioid agonist indicated in adults for ...The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records.

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