Lunesta
Product Images NDC 68258-7049

3 FDA label images from Dispensing Solutions, Inc. · 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 Lunesta (NDC 68258-7049). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Ndc 68258-7048-xx (Ndc 68258 7048 Xx Sepracor)

Ndc 68258-7048-xx (Ndc 68258 7048 Xx Sepracor)
DispenseQuick label for Lunesta 2 mg tablets, manufactured for Sepracor Inc. The label includes active ingredient eszopiclone 2 mg per tablet, NDC 68258-7048-XX, and product number 7048-X. Instructions note to take orally at bedtime or as directed, avoid alcohol, and that the drug may cause drowsiness. The label also contains lot number SAMPLE, expiration 00-00, and an RX number, with warnings and dispensing information by Dispensing Solutions, Inc.*
FDA Label Image

Ndc 68258-7049-xx (Ndc 68258 7049 Xx Sepracor)

Ndc 68258-7049-xx (Ndc 68258 7049 Xx Sepracor)
Lunesta 3 mg tablet label from Dispensing Solutions, Inc. Includes prescription details, dosage strength, and active ingredient eszopiclone. The label features dosing instructions, warnings about drowsiness and alcohol use, and packaging information with NDC and lot numbers. It also shows storage instructions and legal cautions.*
FDA Label Image

Chemical Structure (Lun00 0013 01)

Chemical Structure (Lun00 0013 01)
Chemical structure of Lunesta (eszopiclone), showing its molecular configuration with labeled atoms including nitrogen, oxygen, and chlorine within rings and attached groups.*

* 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.