Product Images Clopidogrel Bisulfate

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Product Label Images

The following 10 images provide visual information about the product associated with Clopidogrel Bisulfate NDC 63739-178 by Mckesson Corporation Dba Sky Packaging, 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.

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Each tablet of the medication contains 391.5 mg of clopidogrel in bisulfate USP. The dosage and storage information can be seen in the package insert. The unit-dose package is not child-resistant. This medication is for institutional use only. The NDC number is 63739-178-30. For further information about the medication, please visit the website mentioned. The rest of the text is not readable.*

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This appears to be a table or graph displaying the effects of different proton pump inhibitors (PPIs) on the active metabolite AUC (area under the curve) when co-administered. The PPIs listed are Dexlansoprazole (60 mg), Lansoprazole (30 mg), Pantoprazole (80 mg), and Omeprazole (80 mg). The symbols "T T T T" might indicate statistical significance or dosage timing, but without additional context, it is not possible to determine their meaning.*

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This is a chart comparing the efficacy of two drugs, Placebo (+ aspirin) and Clopidogrel (+ aspirin), over the course of several months. The chart displays the cumulative event rate (%) and the months of follow-up. Other standard therapies were used alongside the drugs as needed.*

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This appears to be a comparison of two treatments, "Placebo" and "Clopidogrel," in terms of their impact on mortality rates. The data shows that there were 1845 deaths (8.1%) in the placebo group and 1726 deaths (7.5%) in the clopidogrel group. Additionally, the latter had a 7% proportional risk reduction (p=0.03). The time period of the study ranged from 0 to 28 days after randomization.*

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This text reports the results of a study evaluating the effectiveness of Clopidogrel in reducing the risk of death, reinfarction, or stroke before the first discharge after an event. The study was conducted with 2310 participants receiving a placebo, of which 10.1% experienced an adverse event, and 2121 participants receiving Clopidogrel, of which 92% experienced a similar event. The text reports a proportional risk reduction of 9% for the group receiving Clopidogrel, and the statistical significance of this outcome (p=0.002). The data is presented over the time since the participants were randomized, up to 28 days.*

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The text is discussing Clopidogrel and its effectiveness in preventing fatal and non-fatal vascular events.*

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* 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.