Zolpidem Tartrate Tablet, Film Coated
Product Images NDC 60687-838

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 60687-838). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

5 mg Zolpidem Tartrate Tablet Blister (5 mg Zolpidem Tartrate Tablet Blister)

This image shows multiple identical labels for Zolpidem Tartrate 5 mg tablets from American Health Packaging. Each label indicates the tablet is film coated and for oral use, including barcodes, NDC 60687-838, and placeholder text for lot number and expiration date.*

FDA Label Image

5 mg Zolpidem Tartrate Tablets Carton (5 mg Zolpidem Tartrate Tablets Carton)

Zolpidem Tartrate 5 mg film-coated tablets label by American Health Packaging. The label indicates 100 tablets per package with a US Prescription Drug designation and Controlled Substance Schedule IV classification. It includes dosage strength, tablet count, storage instructions, distributor information, and a QR code for medication guide and prescribing information.*

FDA Label Image

Ahp83801

Zolpidem Tartrate 5 mg film-coated oral tablet imprinted with 'E' on one side and '7 8' on the other. The round, white tablet is used for human prescription drug treatment and is labeled by American Health Packaging.*

FDA Label Image

Structural Formula (Structural Formula)

Chemical structure of Zolpidem Tartrate, showing the molecular configuration of zolpidem along with the tartrate moiety. The structure includes aromatic rings, nitrogen atoms, and carboxyl groups characteristic of the salt form.*

* 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.