Zolpidem Tartrate Tablet, Film Coated, Extended Release
Product Images NDC 71610-254

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 71610-254). 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 12.5 mg (71610 0254 30)

Zolpidem Tartrate ER USP 12.5 mg extended release film coated tablets, packaged in a bottle of 30 tablets. The label includes storage instructions, manufacturer details (Sun Pharmaceutical Ind. Ltd., Dadra, India), and the labeler (Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN). It notes the product is prescription only (Rx Only) and warns it may be habit forming.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chemical-structure (Chemical Structure)

Chemical structure diagram of Zolpidem Tartrate, showing the molecular arrangement including indole and phenyl rings along with the tartrate salt components.*

FDA Label Image

Figure1 (Figure1)

A line graph titled 'Mean Plasma Concentration-Time Profiles for Zolpidem Tartrate Extended-Release Tablets (12.5 mg) and Immediate-Release Zolpidem Tartrate (10 mg).' The y-axis shows zolpidem plasma concentrations in ng/mL, ranging from 0 to 120, and the x-axis shows time in hours from 0 to 8. Two lines are plotted: one for the 12.5 mg extended-release tablet (solid circles) and one for the 10 mg immediate-release tablet (open squares), illustrating plasma concentration changes over time.*

* 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.