Dex-moxi-ketor
Product Images NDC 71384-513

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Dex-moxi-ketor (NDC 71384-513). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Imprimis Njof, 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

Package Label (Dex Moxi Ketorboxlabelndc)

Package Label (Dex Moxi Ketorboxlabelndc)
This is a description of a compounded drug with the National Drug Code 71384-513-01. It contains 1 ml/vial with a concentration of 1/0.5[0.4) mglml and is sold in a quantity of 20. The drug was compounded by Imprimis NJOF, LLC and should be stored at a temperature of 20 to 25°C. The expiration date is listed, but the date compounded is not available. The drug is not for resale and in case of an adverse event, the FDA should be contacted.*

* 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.