Zolpidem Tartrate Tablet, Film Coated, Extended Release
Product Images NDC 63187-862

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 63187-862). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure (Zolpidem 01)

Chemical Structure (Zolpidem 01)
Chemical structure of zolpidem tartrate showing two zolpidem molecules complexed with tartaric acid. The structure includes imidazopyridine rings and accompanying tartaric acid moieties.*
FDA Label Image

Figure 1 (Zolpidem 02)

Figure 1 (Zolpidem 02)
A line graph comparing plasma concentration (ng/mL) of zolpidem over time (hours) for 12.5 mg extended-release and 10 mg immediate-release zolpidem tartrate tablets. The graph shows concentration peaking around 1.5 to 2 hours, with extended-release maintaining higher levels over time compared to immediate-release.*
FDA Label Image

63187-862-30 (Zolpidem 04)

63187-862-30 (Zolpidem 04)
Label for Zolpidem Tartrate 12.5 mg extended-release tablets by Proficient Rx LP. The label states prescription use only, schedule IV controlled substance, and contains 30 blue, round, bi-convex, film-coated tablets. It includes product ID PZ086230 and manufacturer information for Winthrop U.S., a Sanofi Aventis U.S. LLC business, stored between 15°–25°C. The label advises dispensing with medication guide and keeping medication out of children’s reach.*

* 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.