· PDF 檔案
Drug recall notice for Losartan Potassium tablets Camber Pharmaceuticals, Inc. makers of Losartan Potassium tablets, is recalling 87 lots of Losartan Tablets USP 25 mg, 50 mg, and 100 mg to consumer level. This recall was prompted due to the detection of trace
D. APO-Losartan / HCTZ 50/12.5 mg Tablet DIN, NPN, DIN-HIM DIN 02371235 Dosage form Tablet Strength Hydrochlorothiazide 12.5mg Losartan potassium 50.0mg Lot or serial number NL1441, NZ8848, NL1445, NZ8849, NZ8860 Recalling Firm Apotex Inc.
27/6/2019 · Losartan potassium tablets sold by Macleods Pharmaceuticals were recalled after trace amounts of a probable carcinogen known as NMBA were found in
Teva Pharmaceuticals USA has expanded its voluntary consumer-level recall originally initiated on April 25, 2019 in the United States of losartan potassium tablets. This expanded recall includes six (6) lots of bulk losartan potassium USP Tablets (two lots of 50 mg
· PDF 檔案
Drug recall notice for Losartan Potassium tablets May 3, 2019 Vivimed Life Sciences Pvt Ltd Issues Voluntary Nationwide Recall of Losartan Potassium 25 mg, 50 mg and 100 mg Tablets, USP Due to the Detection of Trace Amounts of N-Nitroso-N-methyl-4
LOSARTAN POTASSIUM and HYDROCHOLOROTHIAZIDE TABLETS, USP 100 mg/12.5 mg, 1000-count bottles, NDC number 13668-117-10, Lot BX35C023, expiration date 5/2019. Those who may have medical questions about the recall or who want to report a reaction to the medication are being directed to call 1-800-912-9561 or email [email protected].
Product name/Active Pharmaceutical Ingredient (API) DIN Strength Lot Expiry APO-LOSARTAN 02379058 25 mg NL1453 08/2019 APO-LOSARTAN 02379058 25 mg NL1452 08/2019 APO-LOSARTAN 02353504 50 mg NK1254 08/2019 APO-LOSARTAN 02353504
On Jan. 3, the FDA said Torrent Pharmaceuticals has added eight more lots of losartan potassium tablets to its recall list. Losartan potassium is a drug used to treat high blood pressure and is
Hi Lou, I have been on Losartan Potassium 50 mg for some years now, but I began a diet, lost 25kg, I am walking and swimming every day and a big diet change and no alcohol, my blood pressure has dropped to sometimes 90/60. I cut my Losartan by 50% for 3
Losartan, sold under the trade name Cozaar among others, is a medication mainly used to treat high blood pressure. It is also used for diabetic kidney disease, heart failure, and left ventricular enlargement. It is taken by mouth. It may be used alone or in addition to other blood pressure medication. Up to six weeks may be
Medical uses ·
Torrent Pharmaceuticals Limited has expanded its recall of Losartan potassium tablets USP. Originall USP 50mg/12.5 mg, 90-count bottles, NDC number 13668-116-90, Lot BP02C008, expiration date
The recalled blood pressure medication that is part of the now expanded recall includes: 50 mg of Losartan Potassium tablets, USP in 1000 count bottles with an NDC code of 13668-409-10, a batch
Camber Pharmaceuticals is the latest company to recall lots of its losartan, a common heart The Food and Drug Administration says the bottles are from 87 lots of 25-, 50-, and 100 mg potassium
Read more about Lupin recalls blood pressure drug from US on Business Standard. Drug firm Lupin is recalling one batch of Losartan Potassium Tablets, used in treating high blood pressure, from the US market for exceeding permissible impurity level, the US
There has been a recall on Metroprolol. I was on the brand name Toprol XL for about 5 years and never had a problem.-200mg. Then my new coverage was not covering so doctor switched me to Coreg CR-80mg- it seemed to work, although BP was a little elevated. (I
The product can be identified as Losartan Potassium Hydrochlorothiazide, 100 mg/25 mg tablets in 1000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912; Exp. Date 06/2020. It is important to note that this recall encompasses less than 1% of the
Losartan is also connected to rarer but more serious adverse effects. Allergic Reactions: Some people may have allergic reactions to losartan-containing drugs.This might develop into difficulty breathing, hives, swelling of the throat, and more. Fetal Toxicity: In 2014, the FDA updated its black box warning for losartan to include fetal toxicity.
Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 25 mg, 50 mg and 100 mg Due to the Detection of Trace Amounts of N
at 9:31 PM EST – Updated January 5 at 9:50 PM (Gray News) – Torrent Pharmaceuticals has expanded the recall of losartan potassium to include eight additional lots, according to the Food and Drug
· PDF 檔案
Sandoz Losartan 25 mg, 50 mg and 100 mg tablets contain the following amounts of potassium: 2.12 mg (<1 mmol), 4.24 mg (<1 mmol), and 8.48 mg (<1 mmol) respectively. Although Sandoz Losartan tablets contain potassium, this amount is too small to
Each film-coated tablet contains 50 mg of losartan potassium, equivalent to 45.8mg of Losartan. Excipient: 52mg of lactose/film-coated tablet. Film-coated tablet White to off white, round, biconvex, film-coated tablets with breakline on one side and “50” debossing
Losartan Recall Lawsuit In November 2018, the FDA issued a recall of Losartan after detecting trace amounts of the probable human carcinogen N-nitrosodiethylamine (NDEA). This is the third blood pressure drug to have been recalled due to possible cancer risk.
Adult Hypertensive Patients Losartan potassium may be administered with other antihypertensive agents, and with or without food. Dosing must be individualized. The usual starting dose of Losartan potassium is 50 mg once daily, with 25 mg used in patients with
Dosing preparations of Cozaar are 25, 50, and 100 mg tablets. Drug interactions with Cozaar may occur with inhibitors of cytochrome P450, potassium- sparing diuretics, and nonsteroidal anti-inflammatory drugs (NSAIDs). Cozaar should not be used during
The Losartan tablets under recall (FDA) The repackaged lots under recall are Losartan Potassium, USP, 25mg and NDC 68645-577-54; Losartan Potassium, USP, 50mg and NDC 68645-578-54; and Losartan
Losartan Potassium Information, Side Effects, Warnings and Recalls. Cancer Risk Prompts Expanded Blood Pressure Drug Recall – News 9. The U.S. Food and Drug Administration says another heart medicine is being voluntarily recalled after tests showed that it was tainted with a potential
Each film-coated tablet contains 50 mg losartan potassium and 12.5 mg hydrochlorothiazide. Excipient(s) with known effect Each film-coated tablet contains 25.6 mg lactose (as monohydrate). Posology Hypertension Losartan and hydrochlorothiazide is not for use
23/1/2019 · Torrent Pharmaceuticals Limited has expanded its recall of Losartan potassium tablets USP. Originally the company recalled 10 lots of the medication. Now company officials have
News Torrent Pharmaceuticals Limited expands recall of Losartan potassium tablets Patients taking the medication should continue as the risk of harm to their health could be higher if discontinued without an alternative The recall is expanding from two lots to 10
Losartan tablets are available in 25 mg, 50 mg, or 100 mg. The usual starting dose is 50 mg, but people treated with diuretics may be started off with 25 mg, once or twice daily. The effects are
Losartan Recall Class Action Lawsuit March 1, 2019 – New Jersey-based Camber Pharmaceuticals, Inc. has issued a nationwide recall for 87 lots of the blood pressure medication Losartan to the consumer level after routine tests found the product to be contaminated with
· PDF 檔案
NEW ZEALAND DATA SHEET 1. PRODUCT NAME LOSARTAN ACTAVIS (Losartan Potassium 12.5mg, 25mg, 50mg and 100mg Tablets) 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each film-coated tablet contains: 12.5 mg losartan potassium 3.
Class 2 Medicines recall: Accord Healthcare Limited – Losartan Potassium 50mg Film-coated Tablets, PL 20075/0022 and Losartan Potassium 100mg Film-coated Tablets, PL 20075/0023 Further to
The starting dose of losartan for pediatric patients 6 years of age or older is 0.7 mg/kg up to 50 mg once daily. Doses more than 1.4 mg/kg or 100 mg daily have not been Losartan may be given with or without food.evaluated in pediatric patients.
Losartan potassium oral tablet, Zydus, 50 mg, bottle, 1000 count, NDC 68382-0136-10 Reason for the Shortage Beginning in mid-2018, FDA found that several angiotensin II receptor blocker (ARB) medicines contained nitrosamine impurities and have been recalled
Losartan and Hydrochlorothiazide oral tablet, Teva, 50 mg/ 12.5 mg, bottle, 1000 count, NDC 00093-7367-10 Reason for the Shortage Beginning in mid-2018, FDA found that several angiotensin II receptor blocker (ARB) medicines contained nitrosamine impurities and have been recalled because they do not meet FDA’s safety standards.
· PDF 檔案
Page 1 of 4 PATIENT INFORMATION LOSARTAN POTASSIUM TABLETS USP 25 mg, 50 mg, 100 mg Rx only Read the Patient Information that comes with losartan potassium tablets before you start taking it and each time you get a refill. There may be new
· PDF 檔案
Continued . . . Torrent – Recall of losartan • On January 3, 2019, Torrent announced a voluntary, consumer-level recall of some lots of losartan tablets due to the detection of trace amounts of an unexpected impurity, identified as N-nitrosodiethylamine (NDEA
Each green, teardrop-shaped, slightly arched tablet, engraved “50” on one side, plain on the other, contains 50 mg losartan as losartan potassium. Nonmedicinal ingredients: lactose monohydrate, magnesium stearate, microcrystalline cellulose, and coating:
Ezetimibe 10 mg tablets and Losartan Potassium 50 mg tablets Voluntary Recall 8/28/2019 Gamunex-C 10% Voluntary Recall 8/22/2019 Relpax Voluntary Recall 8/15/2019 Xeljanz® and Xeljanz XR Black Box Warning 7/26/2019 Fluorouracil Injection Recall 7/24
The recall is expanding from 10 lots of Losartan potassium tablets USP to include six lots of Losartan potassium and hydrochlorothiazide tablets, USP due to detection of trace amounts of an unexpected impurity, FDA said. The products may contain N
Losartan Potassium 50 mg Film Coated Tablet Bottle 1,000 Tablets Aurobindo Pharma 65862020299 Call Us Medical professionals, medical facility employees, individuals paying with Medicaid or private insurance 855.571.2100 Need help with SupplyManager?
Camber Pharmaceuticals manufacturers Losartan, 50 mg- Cozaar Generic- with quality and integrity. A cardiovascular agent used to treat high blood pressure (hypertension) and to help protect the kidneys from damage due to diabetes.
Vivimed Life Sciences issued a recall for 19 lots of losartan potassium tablets after detecting a potentially carcinogenic impurity. To receive the latest hospital and health system business and
DailyMed: Losartan Potassium The information contained on this site is for informational purposes only, and should not be used as a substitute for the advice of a professional health care provider. Please check with the appropriate physician regarding health
· PDF 檔案
COZAAR is available as tablets for oral administration containing either 25 mg, 50 mg or 100 mg of losartan potassium and the following inactive ingredients: microcrystalline cellulose, lactose hydrous, pregelatinized starch, magnesium stearate, hydroxypropyl
Torrent Pharmaceuticals Limited is recalling 60 lots of Losartan potassium tablets and 54 lots of Losartan potassium Blood pressure medication recall expands again to include losartan Blood
Losartan/hydrochlorothiazide can increase the levels of a substance called potassium in your blood. Taking losartan with drugs The starting dose is 50 mg losartan/12.5 mg hydrochlorothiazide
4/7/2019 · Addition of a low dose of hydrochlorothiazide (12.5 mg) to losartan 50 mg once daily resulted in placebo- adjusted blood pressure reductions of 15.5/9.2 mmHg. Analysis of age, gender, and race subgroups of patients showed that men and women, and patients
This company took the API losartan from Zhejiang HuaHai in China, added hydrochlorothiazide from goodness knows where and turned these chemicals into Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25 mg.