Zolpidem Tartrate Tablet, Coated
Product Images NDC 70518-3739

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 70518-3739). 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.

FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Zolpidem Tartrate 10 mg coated tablets packaging label showing 30 tablets per bottle. The label includes regulatory information such as RX only status, NDC number 70518-3739-00, and scheduling as C-IV. Manufacturer listed as Sandoz Inc., Princeton, NJ, with repackaging by RemedyRepack Inc. The label advises storage conditions and cautions on drug transfer restrictions.*
FDA Label Image

Chemical Structure (Zolpidem 01)

Chemical Structure (Zolpidem 01)
Chemical structure of Zolpidem Tartrate, showing the molecular arrangement of its components as depicted in the image, including the tartaric acid salt form.*

* 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.