Recall simvastatin

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  • ” Mar 13, 2023 · SIMVASTATIN Recall D-0411-2023
  • The risk of very serious side effects is extremely low
  • 65862-053-90
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  • It is used to lower triglycerides
  • 05/31/2024 B1822C exp
  • stomach discomfort, upset, or pain
  • Early Communication About an Ongoing Safety Review of Ezetimibe/Simvastatin (marketed as Vytorin), Simvastatin (marketed as Zocor) and Ezetimibe (marketed as Zetia) - FDA

    SIMVASTATIN is a generic drug for cholesterol lowering that was recalled by Accord Healthcare, Inc

    05/31/2023 F0322G exp

    By Linda Carroll

    The product is labeled as Clopidogrel tablets USP 75 mg but may contain Clopidogrel 75mg or Simvastatin Tablets USP 10 mg

    Dr Reddy's Laboratories has initiated a recall of certain strengths of its cholesterol-lowering drug, simvastatin, in the US following concerns over 'chemical contamination' of the product

    All Local Government Units (LGU) and Law Enforcement Agencies (LEAs) are requested to ensure that the Drug Recall

    Of course, statins inhibit the production of cholesterol–they do this very well

    Simvastatin belongs to the group of medicines called HMG-CoA reductase inhibitors, or statins

    Simvastatin tablets USP are an HMG-CoA reductase inhibitor indicated: ()To reduce the risk of total mortality by reducing risk of coronary heart disease death, non-fatal myocardial infarction and stroke, and the need for coronary and non-coronary revascularization procedures in adults with established coronary heart disease

    Popular statins include atorvastatin ( Lipitor ), rosuvastatin (Crestor), and simvastatin (Zocor)

    They are marketed For any questions regarding this recall, contact Accord Healthcare, Inc

    Simvastatin belongs to the group of medicines called HMG-CoA reductase inhibitors, or statins

    Phone: 877-566-6108 · Fax: 817-868-5362 · rxrecalls@inmar

    As a result, less cholesterol is made and levels of cholesterol in the blood decrease

    lack or loss of strength

    The last Recall Enforcement Report for Simvastatin with NDC 16729-004 was initiated on 02-07-2023 as a Class II recall due to cgmp deviations: recalling drug products following an fda inspection

    Multi event Drug Recall Enforcement Report Class II voluntary initiated by Direct Rx, originally initiated on 03-13-2023 for the product Glimepiride, USP, 4 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0250-30; b) 90-count bottle, NDC 61919-0250-90 Packaged and Distributed By: Direct Rx taking simvastatin 80 mg compared with other statin therapies with similar or greater LDL cholesterol lowering efficacy, and with lower doses of simvastatin

    The last Recall Enforcement Report for Ezetimibe And Simvastatin with NDC 43598-743 was initiated on 10-05-2021 as a Class II recall due to failed excipient specifications; product manufactured using an excipient found to be oos for conductivity The latest recall number for this product is D-0082-2022 and the recall is currently terminated as of 02-16-2023

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