Diclofenac Sodium And Misoprostol Tablet, Delayed Release
Product Images NDC 68001-232

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium And Misoprostol (NDC 68001-232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Image 1

Each Tablet and UsesSee accompanying medication guide. This text also includes some drug and dosage information but it is incomplete and not entirely readable. The text also includes a serialization coding area.*

FDA Label Image

Image 2

This is a description for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, USP. It contains 75 mg diclofenac sodium, USP, and 0.2 mg misoprostol, USP per tablet. It is dispensed in a light-resistant container and should be stored at a controlled room temperature. The medication guide is provided on the packaging. It is contraindicated for pregnant women and could cause harm to the fetus. The NDC number is 68001-232-06.*

* 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.