Divalproex Sodium
Product Images NDC 58118-0040

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 58118-0040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Divalproex Dr 250mg

This is a label of Valproex Sodium DR 250mg tablets which includes information such as the IDC, quantity, lot number, batch number, manufacturer name, expiration date, and location of distribution.*

FDA Label Image

Structure (Divalproextablets Figure 01)

FDA Label Image

Comparison Of Percentage Of Patient Separated By Study (Divalproextablets Figure 02)

FDA Label Image

% Reduction In Cps Rate Vs % Of Patients (Divalproextablets Figure 03)

FDA Label Image

% Reduction In Cps Rate Vs % Of Patients (Divalproextablets Figure 04)

FDA Label Image

Mean 4-week Migraine Rates (Divalproextablets Figure 05)

FDA Label Image

Company Logo (Divalproextablets Figure 06)

FDA Label Image

Divalproex Sodium Dr 500mg Tablet 30 Count Blister Card (Divalproextablets Figure 09)

This is a description of a pharmaceutical product, specifically Divalproex Sodium DR 500mg tablets. The product has a NDC number of 58118-0042-8 and a Mig. NOC number of 29300-0140-05, with a GTIN of 0035818004281. The lot number is SAWPLE123 B SAWPLES058. The tablets were manufactured by Unichem Pharmaceuticals and have an expiration date of September 2018. The location of production is Hasbroek Heights, W, USA, 07604, and its specifications suggest that it may be used for clinical treatment purposes.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.