Eszopiclone
Product Images NDC 50436-3384

View Photos of 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 Eszopiclone (NDC 50436-3384). 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

Eszopiclone-chemical-structure (Eszopiclone Chemical Structure)

Eszopiclone-chemical-structure (Eszopiclone Chemical Structure)
Chemical structure of the active ingredient Eszopiclone, showing its molecular rings and functional groups. The diagram includes nitrogen atoms, carbonyl groups, and a chlorine-substituted pyridine ring, reflecting the compound's detailed skeletal formula.*
FDA Label Image
FDA Label Image

Label Image (Lbl504363383)

Label Image (Lbl504363383)
Eszopiclone 2 mg 30 tablet carton label from Unit Dose Services. The label displays the product name, strength, quantity, and manufacturer Glengmark Pharm Limited, India. It includes dosing instructions, storage conditions, and lot and expiration date placeholders. The packaging has tamper-resistant closure warnings and barcodes.*
FDA Label Image

Label Image (Lbl504363384)

Label Image (Lbl504363384)
Eszopiclone 3 mg tablets in a package of 30, labeled by Unit Dose Services, LLC. The blister card includes NDC 50436-3384-1 and instructions for pharmacists to dispense the medication guide. Manufacturer is Glenmark Pharma Limited, located in India, with MFG NDC 68462-384-01. The label indicates prescription only (Rx Only) status and storage instructions.*

* 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.