Zolpidem Tartrate Tablet, Film Coated, Extended Release
Product Images NDC 68788-8376

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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 68788-8376). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals 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

Zolpidem Tartrate Er Tab 125mg (625fad5b 8817 4773 A2fc 20b662140e6e 00)

Zolpidem Tartrate Er Tab 125mg (625fad5b 8817 4773 A2fc 20b662140e6e 00)
Label for Zolpidem Tartrate ER Tab 12.5 mg, an extended-release film-coated tablet generic for Ambien. The label shows dosage strength, manufacturer as Sun Pharmaceuticals Industries, Inc., storage instructions, and warnings including a caution against alcohol consumption. The label also includes bilingual (English and Spanish) medication directions and a barcode.*
FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of Zolpidem Tartrate showing the molecular arrangement with two molecules of zolpidem linked to tartaric acid.*
FDA Label Image

Figure1 (Figure1)

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).' It shows plasma concentrations (ng/mL) on the y-axis and time (hours) on the x-axis, comparing 12.5 mg extended-release (filled circles) and 10 mg immediate-release (open squares) zolpidem tartrate tablets over 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.