Product Images Divalproex Sodium
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Product Label Images
The following 6 images provide visual information about the product associated with Divalproex Sodium NDC 33261-641 by Aidarex Pharmaceuticals Llc, 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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This text provides information on two studies conducted for the drug named Placebo DVPX. In both studies, participants were given divalproex sodium delayed-release tablets at different doses. In Study 1, the mean dose administered was 1087 mg/day. Study 2 administered doses of either 500 mg/day or 1000 mg/day. DVPX is explained as the abbreviation for the drug divalproex sodium delayed-release tablets.*
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This document appears to be a graph that shows the percentage reduction in CPS (central pain syndrome) rate in patients taking Divalproex sodium delayed-release tablets. The graph displays two bars, indicating that no improvement was seen in 50% of patients and worsening was observed in 2% of patients.*
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This is a description of a medication named Divalproex Sod. DR. The manufacturer is Sun Pharmaceuticals Industries Ltd. in Mumbai, India. The medication comes in the form of delayed-release tablets, with each tablet containing 250 mg of valproic acid as its active ingredient. There are 30 tablets per bottle. The NDC codes for this medication are 83261-0841-50 and 33261-0841-30. The second NDC code corresponds to the generic form of the medication, which is used to treat a variety of conditions, including epilepsy and bipolar disorder.*
* 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.