Ambien Tablet, Film Coated
Product Images NDC 0713-5401

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 0713-5401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette Pharmaceuticals, 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

Chemical Structure (Ambien 01)

Chemical Structure (Ambien 01)
Chemical structure diagram showing the molecular structure of zolpidem tartrate, including the zolpidem component on the left and the tartrate acid structure on the right.*
FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Principal Display Panel (5 mg Tablet Bottle Label)
Ambien 5 mg film-coated tablets label by Cosette Pharmaceuticals, Inc. The label states the active ingredient zolpidem tartrate with dosage strength of 5 mg in oral tablet form. It includes instructions to dispense with a medication guide and indicates prescription use only. The package contains 100 tablets and features a pink and white design with barcode and labeling details.*
FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Principal Display Panel (10 mg Tablet Bottle Label)
Packaging label for Ambien 10 mg film-coated tablets by Cosette Pharmaceuticals, Inc. The label includes the proprietary name Ambien with the generic name zolpidem tartrate, the strength of 10 mg, and a count of 100 tablets. It also notes that the product is prescription only and includes storage and dispensing instructions, along with an NDC barcode and number.*

* 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.