Zolpidem Tartrate Tablet, Film Coated, Extended Release
Product Images NDC 71610-770

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 71610-770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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.

FDA Label Image

Bottle Label 6.25 mg (71610 0770 15)

Zolpidem Tartrate ER 6.25 mg extended-release film-coated tablets carton containing 15 tablets. The label includes storage instructions between 20-25 degrees Celsius, a note to keep the product out of children’s reach, and manufacturing details by Winthrop U.S. in Bridgewater, NJ. The labeler is Aphena Pharma Solutions - Tennessee, LLC, located in Cookeville, TN. The package shows the NDC 71610-0770-15 and contains batch and expiration information.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chemical Structure (Zolpidem 01)

Chemical structure of zolpidem tartrate, showing the molecular arrangement of the zolpidem moiety bonded with the tartrate component. The structure includes the indole ring system and the tartrate's carboxyl and hydroxyl functional groups.*

FDA Label Image

Figure 1 (Zolpidem 02)

A pharmacokinetic curve graph comparing zolpidem plasma concentrations over time for 12.5 mg Ambien-CR and 10 mg zolpidem tartrate immediate release tablets. The x-axis represents time in hours, and the y-axis shows plasma concentration in ng/mL, illustrating differences in drug concentration profiles between the two formulations up to 8 hours.*

* 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.