Edluar Tablet
Product Images NDC 0037-6010

3 FDA label images from Viatris Specialty 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 Edluar (NDC 0037-6010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viatris Specialty 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

Chemical Structure Of Zolpidem Tartrate (Edluar Figure 1)

Chemical Structure Of Zolpidem Tartrate (Edluar Figure 1)
Chemical structure diagram showing the molecular structure of Zolpidem Tartrate, the active ingredient in Edluar tablets. The diagram includes the two components of the tartrate salt form.*
FDA Label Image

Edluar Sublingual Tablets 5 mg Carton Label (Image 01)

Edluar Sublingual Tablets 5 mg Carton Label (Image 01)
Edluar 5 mg sublingual tablets packaging label showing a box for 30 tablets of Zolpidem Tartrate. The label includes directions for sublingual placement, manufacturer information for Meda Pharmaceuticals Inc., storage instructions, and a note for pharmacists to dispense the accompanying Medication Guide. The labeler is Viatris Specialty LLC.*
FDA Label Image

Edluar Sublingual Tablets 10 mg Carton Label (Image 02)

Edluar Sublingual Tablets 10 mg Carton Label (Image 02)
Packaging label for Edluar 10 mg sublingual tablets, containing zolpidem tartrate, from Viatris Specialty LLC. The label indicates the tablet count as 30 sublingual tablets per container. It includes directions for use under the tongue and advises pharmacists to dispense an accompanying medication guide. The label also lists storage instructions and manufacturing 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.