Zolpidem Tartrate
Product Images NDC 55648-715

3 FDA label images from Wockhardt Limited · 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 55648-715). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wockhardt Limited, 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

Container Label 100 T (Zolpidemtarttab M Figure 01)

Container Label 100 T (Zolpidemtarttab M Figure 01)
Label for Zolpidem Tartrate Tablets 5 mg, containing 100 tablets. The label shows the NDC 64679-714-01 and indicates Rx only status. It is manufactured by Wockhardt Limited, Mumbai, India, and distributed by Wockhardt USA LLC, New Jersey, USA. The label includes storage instructions and a pharmacy dispensing note.*
FDA Label Image

Container Label 1000 T (Zolpidemtarttab M Figure 02)

Container Label 1000 T (Zolpidemtarttab M Figure 02)
Zolpidem Tartrate 10 mg tablets packaging label from Wockhardt Limited, containing 1000 tablets. The label includes storage instructions, NDC number 64679-715-02, and advises pharmacists to dispense with medication guide. Distributed by Wockhardt USA LLC, the label features a barcode, indicates non-varnish area for printing, and shows a child-resistant container warning.*
FDA Label Image

Structure (Zolpidemtarttab M Figure 03)

Structure (Zolpidemtarttab M Figure 03)
Chemical structure diagram showing the molecular structure of zolpidem tartrate, with two main molecular components illustrated.*

* 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.