Divalproex Sodium Tablet, Film Coated, Extended Release
Product Images NDC 70518-4553
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 70518-4553). 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.
Image (546b07bd 7dba 49c9 8caf 7914600d4d19 02)
Image (546b07bd 7dba 49c9 8caf 7914600d4d19 03)
This text appears to describe a chart or graph showing the reduction in CPS (presumably clinical pharmacy services) rate based on different percentages. The table may present percentages ranging from 100% to 2%, including categories like "No change", "High Dose Divalproex Sodium Delayed-Release Tablets" and "Low Dose Divalproex Sodium Delayed-Release Tablets". It also mentions the percentage of patients involved in this reduction analysis.*
Image (546b07bd 7dba 49c9 8caf 7914600d4d19 04)
Remedy_label (Remedy Label)
This text provides information about Divalproex Sodium tablets manufactured by Unichem Labs Ltd. in Goa, India. The tablets are extended-release and come in a pack of 30 tablets with a dosage of 500 mg. The usual dosage instructions are included in the insert. The medication should be stored at a temperature of 20-25°C (68-77°F) with excursions allowed to 15-30°C (59-86°F). The lot number and expiration date are missing from the text. The tablets were repackaged by RemedyRepack, a company located in Indiana, PA, with a contact number provided.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.