Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 68180-780

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 68180-780). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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 of Zolpidem Tartrate, showing its molecular arrangement including multiple benzene rings and functional groups typical to the tartrate salt form.*

FDA Label Image

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A pharmacokinetic curve comparing zolpidem plasma concentrations (ng/mL) over time (hours) for 12.5 mg zolpidem tartrate extended-release tablets versus 10 mg zolpidem tartrate immediate release. The graph shows plasma levels rising rapidly for both, with extended-release maintaining higher levels longer than immediate release.*

FDA Label Image

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Label for Zolpidem Tartrate Extended-Release Tablets USP 6.25 mg, oral extended-release tablets in a package of 30. Label highlights pharmacist instructions to dispense medication guide and includes storage and dosage directions. Manufactured by Lupin Limited and labeled by Lupin Pharmaceuticals, Inc.*

FDA Label Image

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Label for Zolpidem Tartrate Extended-Release Tablets USP, 12.5 mg, oral tablet dosage form. The label states it contains 30 tablets per bottle. Manufactured by Lupin Pharmaceuticals, Inc. and Lupin Limited. Includes storage instructions, pharmacist dispensing guidance, and a QR code for medication guide access.*

* 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.