Divalproex Sodium Tablet, Delayed Release
Product Images NDC 67046-1647

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 67046-1647). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coupler 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.

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FDA Label Image

Label (69452 435 30 Divalproex Dr 500mg 67046 1647 30)

Label (69452 435 30 Divalproex Dr 500mg 67046 1647 30)
This product is Divalproex Sodium, a medication available in tablet form containing 500mg (DR). This prescription medication is used for specific medical purposes and should only be used as directed by a healthcare professional. The tablets are enteric-coated and delayed-release, containing Divalproex Sodium USP equivalent to Valproic Acid 500mg. It is important to follow the storage instructions provided, store at 20-25°C (68-77°F), and protect from light. Detailed prescribing information can be found in the enclosure provided with the packaging. The batch number, expiration date, and additional contact information for the manufacturer are also included.*

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