Divalproex Sodium Capsule, Delayed Release
Product Images NDC 0904-6615

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 0904-6615). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Figure1 (Figure1)

FDA Label Image

Figure2 (Figure2)

FDA Label Image

Carton Label (Image 01)

Carton Label (Image 01)
This is a pharmaceutical product containing 100 sprinkle capsules of divalproex sodium, a medication used to treat certain types of seizures and mood disorders. The product is meant to be dispensed with a medication guide by a pharmacist. The capsules are delayed-release and come in a unit dose pack. The National Drug Code (NDC) for this product is 0904-6615-61.*
FDA Label Image

Picture1 (Picture1)

FDA Label Image

Picture2 (Picture2)

FDA Label Image

Picture3 (Picture3)

FDA Label Image

Picture4 (Picture4)

FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.