Product Images Divalproex Sodiumdelayed-release Delayed-release
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Product Label Images
The following 6 images provide visual information about the product associated with Divalproex Sodiumdelayed-release Delayed-release NDC 33261-621 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.
This figure shows the percentage of patients in Study 1 and Study 2 who achieved a greater than 30% reduction in symptom score from baseline. The results indicate that in both studies, 60% of patients treated with divalproex sodium (DVPX) were able to achieve this level of improvement. Placebo (PBO) was used as a comparison drug. The asterisk indicates that the results were statistically significant (p < 0.05).*
The text represents a graph showing the reduction in CPS rate for patients taking Divalproex Sodium compared to placebo. The graph shows the percentage reduction in CPS rate ranging from -100% to 100%. The figure also includes a bar chart showing the percentage of patients who experienced improvement, no change, or worsening while taking Divalproex Sodium.*
This is a graph (Figure 3) that shows the percentage reduction in CPS (Chronic Pain Score) rate for patients who were given either a high or low dose of a particular treatment. The graph shows that those who received the high dose experienced a greater reduction in CPS rate than those who received a low dose. The graph also shows the percentage of patients who experienced improvement, no change, or worsening of their CPS rate.*
The text describes Figure 4 which presents the mean 4-week migraine rates for two studies, one with placebo and one with divalproex sodium. The mean dose of divalproex sodium in Study 1 was 1,087 mg/day, while in Study 2 it was either 500 or 1,000 mg/day.*
This package insert contains cautionary statements about dispensing the medication without a prescription and storing it in a controlled room. The medication contains Divalproex Sodium with 500mg strength and has 60 tablets in the bottle. The manufacturer and distributor of this medication are Aidarex Pharmaceuticals LLC and Qualitest Pharmaceuticals, respectively. The NDC number for this medication is 33261-0621-60. The package insert includes a chart with instructions for taking the medication.*
* 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.