Emend
Product Images NDC 0006-3941

3 FDA label images from Merck Sharp & Dohme Corp. · 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 Emend (NDC 0006-3941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Merck Sharp & Dohme Corp., 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

Chemical Structure (Emend Iv 01)

Chemical Structure (Emend Iv 01)
Chemical structure of the active ingredient in EMEND by Merck Sharp & Dohme Corp., depicting a complex molecule with multiple rings, fluorine, trifluoromethyl groups, and phosphate and amino acid components.*
FDA Label Image

Principal Display Panel (Carton 115 mg)

Principal Display Panel (Carton 115 mg)
Packaging label for Emend 115 mg injection by Merck Sharp & Dohme Corp. The label indicates fosaprepitant dimeglumine as the active ingredient, provided as a sterile lyophilized powder for intravenous use. It includes preparation instructions, storage conditions, and warnings against certain solutions. The package contains one single-dose 115 mg vial.*
FDA Label Image

Principal Display Panel (150 mg Vial Carton)

Principal Display Panel (150 mg Vial Carton)
Emend 150 mg per vial (fosaprepitant dimeglumine) injection carton label by Merck Sharp & Dohme Corp. The label indicates a sterile lyophilized powder for intravenous use after reconstitution and dilution, single-dose vial. Storage instructions specify refrigeration at 2°C to 8°C. Includes inactive ingredients and warnings about incompatible solutions.*

* 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.