Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 76420-319

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 76420-319). 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

Zolpidem Tartrate (39503a0f Bbf2 4bb4 Ab5d 118d2e3b5bbf 01)

Zolpidem Tartrate (39503a0f Bbf2 4bb4 Ab5d 118d2e3b5bbf 01)
Chemical structure of Zolpidem Tartrate, showing the molecular configuration including aromatic rings, nitrogen atoms, and tartrate moiety.*
FDA Label Image

Im-2 (39503a0f Bbf2 4bb4 Ab5d 118d2e3b5bbf 02)

Im-2 (39503a0f Bbf2 4bb4 Ab5d 118d2e3b5bbf 02)
A pharmacokinetic graph illustrating 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 concentration changes from 0 to 8 hours post-dose for both formulations, highlighting differences in release profiles.*
FDA Label Image

Label (Label 12 5mg)

Label (Label 12 5mg)
Multiple packaging labels for Zolpidem Tartrate ER Tablets USP 12.5 mg by Enovachem Pharmaceuticals. Labels show various quantities: 30, 60, 90, and 100 tablets. The tablets are described as blue, round, biconvex, film-coated, and debossed. Each label includes NDC numbers, storage instructions (20-25°C), drug schedule (CIV), and cautions about prescription and child safety.*
FDA Label Image

6.25mg (Label 6 25mg)

6.25mg (Label 6 25mg)
Labels for Zolpidem Tartrate extended release tablets 6.25 mg from Enovachem Pharmaceuticals, packaged in quantities of 30, 60, 90, and 100 tablets. The labels include NDC codes, storage instructions, controlled substance classification (CIV), and manufacturer details for Lupin Pharmaceuticals, Inc. Each label features a QR code and batch/expiration fields.*

* 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.