Product Images Losartan Potassium
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Product Label Images
The following 6 images provide visual information about the product associated with Losartan Potassium NDC 71205-226 by Proficient Rx Lp, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
71205-226-30 - 8ca0c9d3 3a50 4efe 92df 30a0c50d48a7 06
This is a description of Losartan Potassium medication manufactured by Zhejang Huahai Pharmaceutical Co.Ltd. The medication is a prescription-only type and is packaged in a white-to-off-white film-coated tablet form. Each tablet contains 25mg of Losartan Potassium, USP ot PR. The lot number is EW000000 and the product ID is SL022690. It is recommended to store the medication at 20°C-25°C (68°F-77°F). It is important to keep the medication out of reach of children.*
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This appears to be a comparison of two medications, Atenolol and Losartan Potassium. It shows a percentage of patients with a primary endpoint and an adjusted risk reduction of 13% with a p-value of 0.021. The graph shows study data for a period of 66 months.*
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This text appears to compare the medication Atenolol with Losartan Potassium in terms of adjusted risk reduction, where Losartan Potassium has shown a 25% risk reduction compared to Atenolol. The percentage of patients with fatal/non-fatal stroke over a period of 66 months has also been recorded. No further information is available to provide a context for this data.*
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This is a table presenting the primary endpoint events for different demographic subgroups in clinical trials comparing the efficacy of Losartan Potassium and Atenolol. The primary composite endpoint is stroke (fatal/non-fatal). The subgroups are defined by age, gender, race, ISH, diabetes, and history of CVD. The table includes the number of events, event rate, and hazard ratio (95% CI) for each subgroup. The symbols in the table are proportional to the sample size. The text also mentions that the results were adjusted for baseline Framingham risk score and level of electrocardiographic left ventricular hypertrophy.*
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This seems to be a chart showing the percentage of patients with an event over a 48 month period. The chart compares the outcomes of patients taking Losartan Potassium versus Placebo. It appears that there was a risk reduction of 16.1% in the Losartan group compared to Placebo. The p-value is reported as 0.022.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.
