Zolpidem Tartrate
Product Images NDC 50436-0008

5 FDA label images from Unit Dose Services · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Zolpidem Tartrate (NDC 50436-0008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Label Image (Lbl504360007)

Label Image (Lbl504360007)
Zolpidem Tartrate 5 mg tablet carton label for a 60-count package. The label indicates each tablet contains 5 mg of zolpidem tartrate USP. Manufactured by Torrent Pharmaceuticals Ltd., India, and packaged by Unit Dose Services, LLC, Florida. The label includes storage instructions, warnings, and place for lot number and expiration date.*
FDA Label Image

Label Image (Lbl504360008)

Label Image (Lbl504360008)
Zolpidem Tartrate 10 mg tablet blister pack containing 30 tablets. Label shows the drug name and strength, manufacturer Torrent Pharmaceuticals Ltd., with an address in India. It includes dispensing instructions, storage information, warnings, lot number, expiration date, and NDC 13668-0008-01. Marked for prescription use only (RX ONLY).*
FDA Label Image

Image 1 (Zolpidemtartratetab Figure 01)

Image 1 (Zolpidemtartratetab Figure 01)
Chemical structure of Zolpidem Tartrate showing the molecular arrangement of the active ingredient.*
FDA Label Image

Image (Zolpidemtartratetab Figure 02)

FDA Label Image

Logo (Zolpidemtartratetab Figure 03)

* 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.