Ambien Tablet, Film Coated
Product Images NDC 0024-5401

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 Ambien (NDC 0024-5401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanofi-aventis U.s. 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

Chemical Structure (Ambien 01)

Chemical Structure (Ambien 01)
Chemical structure diagram showing the molecular structure of zolpidem tartrate, the active ingredient in Ambien. The image displays the arrangement of chemical bonds and atoms, including the tartrate component, relevant to the compound formulation.*
FDA Label Image

Principal Display Panel (5 mg, 100 Tablet Bottle Label)

Principal Display Panel (5 mg, 100 Tablet Bottle Label)
Label for Ambien 5 mg film-coated tablets containing zolpidem tartrate, an oral human prescription drug by Sanofi-Aventis U.S. LLC. The label indicates a package size of 100 tablets and includes storage instructions, dispensing guidance with medication guide, barcode, and relevant product codes.*
FDA Label Image

Principal Display Panel (10 mg, 100 Tablet Bottle Label)

Principal Display Panel (10 mg, 100 Tablet Bottle Label)
Ambien 10 mg film-coated tablets packaging label showing the brand name, generic name (zolpidem tartrate), strength, and tablet count of 100. The label includes instructions to dispense with medication guide, indicates Rx only, and shows the labeler as Sanofi-Aventis U.S. LLC. It also displays storage instructions, NDC number 0024-5421-31, and lot/expiration details.*

* 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.