Zolpidem Tartrate Tablet
Product Images NDC 80425-0301

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 80425-0301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of 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

Structure (Structure)

Chemical structure of zolpidem tartrate, showing the molecular arrangement of the active ingredient zolpidem combined with the tartrate moiety.*

FDA Label Image

Label 1 (Zolpidem 10mg 80425 0301 01)

Zolpidem Tartrate 10 mg tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC, featuring product name, strength, NDC 80425-0301, quantity of 30 tablets, storage instructions (20-25°C), and expiration date 12/31/2025. The label includes a reference to the source NDC 13668-0008-10 and warnings about misuse.*

FDA Label Image

Label 2 (Zolpidem 10mg 80425 0301 02)

Zolpidem Tartrate 10 mg tablet packaging label from Advanced Rx Pharmacy of Tennessee, LLC. The label includes batch and lot information, expiration date of 12/31/2025, a barcode, storage instructions at 20-25°C, and a comparison reference to Ambien. The package contains 60 tablets and is classified as a Schedule IV controlled substance.*

FDA Label Image

Label 3 (Zolpidem 10mg 80425 0301 03)

Zolpidem Tartrate 10 mg tablet label from Advanced Rx Pharmacy of Tennessee, LLC, NDC 80425-0301. The label includes storage instructions (20-25°C), a comparison to Ambien with NDC 80425-0301-03, lot number, expiration date 12/31/2025, a barcode, and a reference to Torrent Pharma. Controlled substance classification C-IV is also shown.*

* 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.