Zolpidem Tartrate Tablet, Film Coated, Extended Release
Product Images NDC 71610-913

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 71610-913). 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 0913 30)

Bottle Label 6.25 mg (71610 0913 30)
Label for Zolpidem Tartrate Extended-Release USP 6.25 mg tablets, containing 30 film-coated tablets. The label includes NDC 71610-913-30, manufacturer information (Sun Pharmaceutical Ind. Ltd., Dadra, India), and repackager details (Aphena Pharma, Cookeville, TN). Storage instructions, warnings, and regulatory classification (C-IV, RX Only) are also present.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of Zolpidem Tartrate, showing the molecular arrangement including two Zolpidem units and the tartaric acid component on the right side.*
FDA Label Image

Figure1 (Figure1)

Figure1 (Figure1)
A line graph showing mean plasma concentration-time profiles for zolpidem tartrate extended-release tablets (12.5 mg) and immediate-release zolpidem tartrate (10 mg). The x-axis represents time in hours, and the y-axis represents zolpidem plasma concentrations in ng/mL, depicting changes in concentration over an 8-hour period for both formulations.*

* 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.