Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 68788-7422

3 FDA label images from Preferred Pharmaceuticals, Inc.. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 68788-7422). 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

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Chemical structure diagram showing the molecular structure of Zolpidem Tartrate, including the zolpidem molecule and the tartrate moiety, as indicated by the connected aromatic and functional groups.*
FDA Label Image

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A line graph comparing zolpidem plasma concentrations (ng/mL) over time (hours) for 12.5 mg zolpidem tartrate extended-release tablets and 10 mg zolpidem tartrate immediate-release tablets. The graph shows plasma concentration on the vertical axis and time on the horizontal axis, illustrating the pharmacokinetic profiles of both formulations over 8 hours.*
FDA Label Image

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The label for Zolpidem Tartrate ER Tab 12.5 mg extended-release oral tablets. It references the generic name Zolpidem Tartrate and mentions it is a controlled substance (CIV). The label shows the product is manufactured by Lupin Pharmaceuticals, Inc. with dosage and warnings about alcohol and dosing interval instructions in both English and Spanish. Preferred Pharmaceuticals, Inc. is indicated as the labeler, with space for lot, batch, expiration date, and product number details.*

* 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.