Diclofenac Sodium And Misoprostol
Product Images NDC 42367-111

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium And Misoprostol (NDC 42367-111). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eagle Pharmaceuticals, 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.

FDA Label Image

Principal Display Panel – 50 mg Bottle Label (Dic06 0002 01)

Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets 50 mg/0.2 mg, a 60-tablet package by Eagle Pharmaceuticals, Inc. The label includes warnings, tablet content details, storage instructions, and manufacturer information indicating the product is Rx only.*

FDA Label Image

Principal Display Panel – 75 mg Bottle Label (Dic06 0002 02)

Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, strength 50 mg/0.2 mg, containing 90 tablets. The label includes a pregnancy-related contraindication warning and storage instructions. Manufactured by Cipla Ltd., India, for Eagle Pharmaceuticals, Inc. It instructs pharmacists to dispense with an attached patient leaflet and medication guide.*

FDA Label Image

Principal Display Panel – 75 mg Bottle Label (Dic06 0002 03)

Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, containing 75 mg/0.2 mg strength. The label indicates a package of 60 tablets, prescription only, distributed by Eagle Pharmaceuticals, Inc. It includes a pregnancy warning and dosage information, manufacturer details from Cipla Ltd., India, 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.