Product Images Atorvastatin Calcium

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Product Label Images

The following 5 images provide visual information about the product associated with Atorvastatin Calcium NDC 68071-4835 by Nucare Pharmaceuticals,inc., 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.

PDP - 68071 4835 6

PDP - 68071 4835 6

This is a label of Atorvastatin Calcium 20mg tablets manufactured by NuCare Pharmaceuticals, Inc. It contains information such as lot number, expiration date, and National Drug Code (NDC) for the product. A warning is given to keep the medication out of reach of children and store it at a controlled temperature between 68-77°F. Consumers are advised to call their doctor for medical advice on any side effects and can report side effects to the FDA by calling 1-800-FDA-1088.*

atorvastatin-fig-1 - atorvastatin fig 1

atorvastatin-fig-1 - atorvastatin fig 1

The text appears to be a graph showing the cumulative incidence in percentage over the course of 35 years for two different treatments, Atorastatin and Placebo, with corresponding values given on the vertical axis from 0% to 40%. The horizontal axis displays the number of years. The graph indicates that Atorastatin has a lower cumulative incidence rate than Placebo over the course of 35 years, with an HR (hazard ratio) of 0.64 and a p-value of 0.00005.*

atorvastatin-fig-2 - atorvastatin fig 2

atorvastatin-fig-2 - atorvastatin fig 2

This is a graph showing the cumulative hazard percentage for a placebo and Atorvastatin. The hazard ratio for Atorvastatin compared to placebo is 0.63 with a confidence interval between 0.48 and 0.83 and a p-value of 0.001. It also shows the time to the first primary endpoint through four years of follow-up.*

atorvastatin-fig-3 - atorvastatin fig 3

atorvastatin-fig-3 - atorvastatin fig 3

This is a table presenting data on the percentage of subjects experiencing a major cardiovascular endpoint after taking atorvastatin at 10 mg or 80 mg. The data shows that the percentage of subjects experiencing the event was 0.2 for both doses, but a higher dose of 80 mg was associated with a lower hazard ratio (0.78) and a p-value of 0.0002. The table also shows the time to the first major cardiovascular endpoint over four years.*

atorvastatin-st - atorvastatin st

atorvastatin-st - atorvastatin st

* 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.