Zolpidem Tartrate Tablet, Film Coated
Product Images NDC 71610-151

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 71610-151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 5 mg (71610 0151 15)

Zolpidem Tartrate USP 5 mg film-coated tablets, package containing 15 tablets. The label includes the drug name, dosage strength, and quantity, and notes storage conditions and manufacturer details. It indicates repackaging by Aphena Pharma Solutions - Tennessee, LLC, with manufacturer listed as Aurobindo Pharma Limited, Mahaboob Nagar, India. The label includes an NDC number and mentions prescription use only.*

FDA Label Image

Bottle Label 10 mg (71610 0152 10)

Label for Zolpidem Tartrate, USP 10 mg film-coated tablets, containing 10 tablets. The label includes a warning that the drug may be habit forming and storage instructions. It lists the manufacturer as Aurobindo Pharma Limited, India, and the repackager as Aphena Pharma Solutions - Tennessee, LLC, USA. It specifies the product is for prescription use only.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Chemical Structure (Zolpidem Str)

Chemical structure diagram showing Zolpidem Tartrate, illustrating the molecular composition including the zolpidem core structure and tartrate moiety.*

* 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.