Zolpidem Tartrate Tablet
Product Images NDC 76420-263

View Photos of 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 76420-263). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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

Label (Label 10mg)

Label (Label 10mg)
Packaging labels for Zolpidem Tartrate Tablets, USP 10 mg, showing two package sizes: quantity 30 and quantity 60 tablets. The labels include National Drug Code (NDC) numbers 76420-263-30 and 76420-263-60, respectively. They indicate the product is manufactured for Torrent Pharma, Inc. and packaged by Enovachem Pharmaceuticals in Torrance, CA. Both labels state the drug status as Schedule CIV and include storage instructions and cautionary text.*
FDA Label Image

Label (Label 5mg)

Label (Label 5mg)
Labels for Zolpidem Tartrate Tablets, USP 5 mg from Enovachem Pharmaceuticals, packaged for Torrent Pharma, Inc. The labels specify two package sizes: 30 tablets (NDC 76420-233-30) and 60 tablets (NDC 76420-233-60). Each label includes a barcode, QR code, drug status (CIV), and storage warnings. Tablets are described as red, capsule-shaped with a debossed logo.*
FDA Label Image

Image 1 (Structure)

Image 1 (Structure)
Chemical structure of zolpidem tartrate, showing the molecular components and arrangement for the active ingredient in ZOLPIDEM TARTRATE tablets by Asclemed USA, Inc.*

* 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.