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Divalproex Sodium
Product Images NDC 70518-3620
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 70518-3620). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Remedyrepack Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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Mm2 (Divalproex Sodium 250mg 70518 3620 01)
Divalproex Sodium is a delayed-release tablet with a strength of 250mg. It is only available with a prescription and should be stored at temperatures between 20-25°C (88-77°F); excursions permitted 15-30°C (59-86°F) [See USP]. The repackaging was done by RemedyRepack Inc., Indiana, PA 15701. For more information on how to use, please refer to the package insert.*
Remedy_label (Remedy Label)
Divalproex Sodium is a medication available in the form of delayed release 250mg tablets, with 100 tablets per box. It can only be obtained with a prescription. The National Drug Code (NDC) for this medication is 70518-3620-00 and the manufacturer is Unichern, Ghaziabad, India 201 003. The medication needs to be stored at 20-25°C (88-77°F) with permitted excursions of 15-30°C (59-86°F). Further instructions can be found in the package insert. The medication has been repackaged by RemedyRepack Inc., Indiana, PA 15701, and it is important to keep all medications out of reach of children.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
