Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 68071-2354

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 68071-2354). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (68071 2354 9)

Packaging label for Zolpidem Tartrate 12.5 mg extended-release tablets by NuCare Pharmaceuticals, Inc. The label indicates #90 tablets in the bottle, manufactured by Lupin Limited, with dosage form as oral extended-release tablets. It includes warnings about habit forming and federal law restrictions, product and lot numbers, and storage instructions to keep at controlled temperatures between 59-86°F.*

FDA Label Image

Zolpidem Tartrate (B0207b5f 53fa 4b2c 8608 4095874aff98 01)

Chemical structure of Zolpidem Tartrate, the active ingredient in ZOLPIDEM TARTRATE 12.5 mg extended-release tablets by NuCare Pharmaceuticals, Inc. The diagram shows the molecular arrangement of the Zolpidem component complexed with tartaric acid.*

FDA Label Image

Im-2 (B0207b5f 53fa 4b2c 8608 4095874aff98 02)

A pharmacokinetic graph showing zolpidem plasma concentrations (ng/mL) over time (hours) comparing 12.5 mg zolpidem tartrate extended-release tablets and 10 mg zolpidem tartrate immediate-release tablets. The graph illustrates concentration levels rising to a peak and then gradually declining for both formulations over an 8-hour period.*

* 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.