Divalproex Sodium Capsule, Coated Pellets
Product Images NDC 70518-1749
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Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Divalproex Sodium (NDC 70518-1749). 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.
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This text provides instructions on how to open and handle a capsule with extra coating to prevent spilling the particles inside. It suggests holding and twisting the capsule carefully to separate the top from the bottom and placing the sprinkles onto a small amount of soft food such as applesauce or pudding before swallowing it altogether without chewing. These instructions should be followed each time before taking the capsule.*
Divalproex Sodium 125mg 70518 1749 00
Divalproex Sodium Sprinkle is a delayed-release capsule containing 125mg. This is a prescription-only medication that is repackaged by RemedyRepack Inc. The NDC number is 70518-1749-00 with an unknown expiration date and LOT number. The source NDC number is 68382-0106-01, and the manufacturer is Zydus Pharm located in Pennington, NJ. The medication should be kept out of reach of children, and the directions for use should be followed as per the package insert. The medication should be stored at temperatures between 20-26°C, with the USP allowing excursions permitted to 15-30°C.*
Remedy_label (Remedy Label)
Divalproex sodium is a delayed-release sprinkle, containing 125 mg in a capsule form. It is available in a quantity of 100 HD2. This drug is distributed by Zydus Pharm in Pennington, N.J. The instructions for use are included in the package insert. It should be stored at 20-26°C (63-77°F), excursions permitted to 15-30°C (59-86°F) [See USP]. RemedyRepack Inc., Indiana, PA 15701, 724.466.8762 repackaged it. It is Rx only and the NDC # is 70518-1749-01. The lot number and expiry of the product should be provided. Keep this medication away from the reach of children.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.