Zolpidem Tartrate Tablet, Film Coated
Product Images NDC 16714-622

3 FDA label images from Northstar Rx Llc · 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 Zolpidem Tartrate (NDC 16714-622). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

Package Label-principal Display Panel (5 mg (100 Tablets Bottle))

Package Label-principal Display Panel (5 mg (100 Tablets Bottle))
Label for Zolpidem Tartrate Tablets USP 5 mg film-coated tablets by NorthStar Rx LLC. The label indicates a 100-tablet count, includes dosage information, storage instructions, manufacturer details, and an over-printing zone with barcode on the right side. Product is made in India and intended for oral use.*
FDA Label Image

Package Label-principal Display Panel (10 mg (100 Tablets Bottle))

Package Label-principal Display Panel (10 mg (100 Tablets Bottle))
Label for Zolpidem Tartrate Tablets, USP 10 mg film-coated tablets. The label indicates Rx only, contains 100 tablets, and is labeled by NorthStar Rx LLC. It includes storage instructions, dosage recommendations, manufacturer information (Aurobindo Pharma Limited, India), and a barcode.*
FDA Label Image

Chemical Structure (Zolpidem Str)

Chemical Structure (Zolpidem Str)
Chemical structure of Zolpidem Tartrate, showing the detailed molecular arrangement of the active ingredient including the zolpidem moiety and the tartrate salt component.*

* 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.