Ambien
Product Images NDC 16590-009

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 16590-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stat Rx Usa 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

Ambien 10 mg Label Image (Ambien 10 mg Label 010)

Ambien 10 mg Label Image (Ambien 10 mg Label 010)
Ambien C-IV 10mg tablet bottle label showing it contains 56 tablets. The label indicates the active ingredient is zolpidem tartrate, with each tablet containing 10mg. It is manufactured by Sanofi-Aventis U.S. LLC in Bridgewater, NJ. The label includes dosing and safety warnings, an NDC number 16590-010-56, and states the product is for prescription use only and should be kept out of reach of children.*
FDA Label Image

Ambien 5 mg Label (Ambien 5 mg Label 009)

Ambien 5 mg Label (Ambien 5 mg Label 009)
Ambien C-IV 5 mg tablet packaging label showing 20 tablets per container. The label states it is a generic for Zolpidem Tartrate. It includes the NDC number 16590-009-20 and manufacturer information for Sanofi-Aventis U.S. LLC, Bridgewater, NJ. The label contains dosage instructions, storage conditions, lot number, and prescription warning to keep out of reach of children. Distributed by STAT Rx USA in Gainesville, GA.*
FDA Label Image

Chemical Structure (Ambien 01)

Chemical Structure (Ambien 01)
Chemical structure diagram related to AMBIEN by STAT Rx USA LLC, showing the molecular components and bonding of its active ingredient.*

* 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.