Zolpidem Tartrate Tablet, Extended Release
Product Images NDC 0781-5315

4 FDA label images from Sandoz Inc · 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 0781-5315). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Zolpidem 01

Zolpidem 01
Chemical structure diagram of zolpidem tartrate showing the molecular arrangement of two zolpidem units and the tartrate molecules as part of the compound.*
FDA Label Image

Zolpidem 02

Zolpidem 02
A line graph comparing zolpidem plasma concentrations (ng/mL) over time (hours) for 12.5 mg zolpidem tartrate extended-release and 10 mg zolpidem tartrate immediate-release formulations. The graph shows plasma concentration rising, peaking, and then declining over an 8-hour period for both formulations, with the extended-release maintaining higher levels later.*
FDA Label Image

Zolpidem 03

Zolpidem 03
Label for Zolpidem Tartrate Extended-Release Tablets USP 6.25 mg oral tablets, containing 30 film-coated extended-release tablets. The label includes dosage details, storage instructions (20° to 25°C), and manufacturer information, Sandoz Inc. The label features a barcode, NDC number 0781-5315-31, and a blue imprint area for dating and lot details.*
FDA Label Image

Zolpidem 04

Zolpidem 04
Label for Zolpidem Tartrate Extended-Release Tablets, USP 12.5 mg, oral dosage form. The label states a package count of 30 tablets and indicates prescription use only. It includes storage instructions, highlights pharmacist guidance on dispensing medication guides, and identifies Sandoz Inc as the labeler with manufacturing by Lek Pharmaceuticals d.d., Slovenia. The label features a barcode, NDC 0781-5316-31, and an imprint area for dating, lot, and expiration details.*

* 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.