Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 63629-4597

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 63629-4597). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 01

Zolpidem 01
Chemical structure diagram showing the molecular structure of Zolpidem tartrate, including its extended chemical composition with constituent atoms and bonds displayed in a two-part format representing the drug's chemical makeup.*
FDA Label Image

Zolpidem 02

Zolpidem 02
A line graph comparing zolpidem plasma concentrations (ng/mL) over time (hours) for 12.5 mg extended-release and 10 mg immediate-release zolpidem tartrate tablets. The graph shows plasma concentration on the y-axis and time in hours on the x-axis, illustrating the extended-release formulation's slower decline in plasma levels compared to the immediate-release tablet.*
FDA Label Image

Lbl636294597

Lbl636294597
Label for Zolpidem ER 12.5 mg extended-release oral tablets, packaged by Bryant Ranch Prepack in Burbank, CA. The label includes the drug classification (CIV), a comparison to Ambien CR 12.5 mg, dosage form, and quantity (30 tablets). It also features storage instructions at 20°-25°C, a warning about possible drowsiness, and the product's NDC number 63629-4597-1.*

* 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.