Zolpidem Tartrate
Product Images NDC 33261-173

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 33261-173). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

Image 1 (Zolpidem Tab Torrent 1)

Image 1 (Zolpidem Tab Torrent 1)
Chemical structure of the active ingredient zolpidem tartrate, showing molecular components and connections.*
FDA Label Image

Logo (Zolpidem Tab Torrent 2)

FDA Label Image

Image Label (Zolpidem Tab Torrent 3)

Image Label (Zolpidem Tab Torrent 3)
ZOLPIDEM TARTRATE 5 mg film-coated tablets packaging label by Aidarex Pharmaceuticals LLC. The label indicates a package size of 30 tablets and includes the statement ‘Generic for Ambien’. It highlights the active ingredient zolpidem tartrate at 5 mg strength per tablet. The label also shows manufacturing information and an NDC number 33261-0172-30.*
FDA Label Image

Image Label (Zolpidem Tab Torrent 4)

Image Label (Zolpidem Tab Torrent 4)
Zolpidem Tartrate 10 mg tablet packaging label by Aidarex Pharmaceuticals LLC. The package contains 30 tablets. The label states the active ingredient per tablet as Zolpidem Tartrate 10 mg. It is indicated as a generic for Ambien, with NDC 33261-0173-30, and includes directions referencing prescription use (RX).*

* 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.