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[PDF File]Losartan Potassium tablets Losartan Potassium tablets,
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URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP October 6, 2016 Page 1 of 1 Dear Valued Customer: This is to advise you of a voluntary recall of 1-lot of NIFEdipine 10 mg Capsules, USP. Specific product information are given in the sections that follow, which details (1) recalled product information, (2) reason for recall, (3) depth of recall,
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[PDF File]Losartan Potassium/Hydrochlorothiazide tablets
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The Health Sciences Authority (HSA) has recalled three brands of high blood pressure medicine which contain losartan – Losartas, Losagen and Hyperten – on 28 March 2019. Seven other brands of losartan medicine approved in Singapore are not affected by the recall. 2. Why are three brands of high blood pressure medicines being recalled?
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[PDF File]Preferred Pharmaceuticals – Recall of losartan
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Losartan Tablets Recalled by AvKARE Product Description NDC # Lot # (Expiration Date) Losartan 25 mg 50268-516-15 19554 (4/2019) Losartan 50 mg 50268-517-15 20121 (6/2019) Due to the large scale and ongoing nature of ARB recalls, certain ARB products, such …
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[PDF File]Recall of 3 brands of Losartan Medicines Frequently Asked ...
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Sandoz Inc. is voluntarily recalling one lot of losartan potassium hydrochlorothiazide tablets, USP 100 mg/25 mg to the consumer level. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (NDEA) contained in the API losartan, USP manufactured by Zhejiang Huahai
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[PDF File]Recall of Losartan by AvKARE Effective Date: April 23, 2019
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Mar 06, 2019 · pharmacy for replacement information, provided information to help them identify if their medication is being recalled, advised to discuss potential alternative therapies with their healthcare provider if they are not able to ... Losartan Tablets Recalled by Camber Product Description NDC # Lot # (Expiration Date) Losartan Tablets 25 mg
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[PDF File]0429-2019-Class 2 Recall Losartan Potassium 25 mg and 100 ...
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Losartan Potassium/Hydrochlorothiazide combination tablets are indicated to treat hypertension and ... being recalled and to notify their sub-accounts. Macleods is arranging for return of all recalled products to Qualanex. Instructions for returning recalled products are given in the recall letter.
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[PDF File]URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP
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Losartan potassium and hydrochlorothiazide tablets 50 mg/12.5 mg, losartan potassium and hydrochlorothiazide tablets 100 mg/12.5 mg, and losartan potassium and hydrochlorothiazide tablets 100 mg/25 mg combine an angiotensin II receptor (type AT1) antagonist and a diuretic, hydrochlorothiazide. Losartan potassium, a non-peptide molecule, is ...
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[PDF File]Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot ...
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Losartan potassium tablets, USP were distributed nationwide to Torrent’s wholesale distributor, repackager and retail customers. Torrent Pharmaceuticals Limited is notifying its distributors and customers by phone and in writing to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts.
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[PDF File]Recall of Losartan by Camber Effective Date: February 28, 2019
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Apr 29, 2019 · and retailers that have product being recalled should immediately stop distribution, quarantine all remaining product in their control, and return the recalled product per the instructions given to them by Golden State Medical Supply. Patients taking Losartan Potassium tablets are advised to continue taking their medication and contact their
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FDA Recalls Yet Another Blood Pressure Medication, Losartan, Due …
All Optum ® trademarks and logos are owned by Optum, Inc. All other brand or product names are trademarks or registered marks of their ... — This recall is being initiated in response to the recall by the manufacturer ( Torrent), which ... related to using the recalled losartan. • Anyone with an existing inventory of the recalled product ...
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Is all losartan being recalled