Diclofenac Sodium And Misoprostol Tablet, Delayed Release
Product Images NDC 42291-233

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 42291-233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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

Label 2 (Screen Shot 2016 09 26 At 11.19.22 Am)

Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, USP 75 mg/0.2 mg by AvKARE. The label indicates 60 tablets in the package, prescription use only. It includes cautionary statements about pregnancy contraindications and storage instructions at 20° to 25°C. The NDC number 42291-2336-0 is also shown with a barcode.*

FDA Label Image

Label 1 (Screen Shot 2016 09 26 At 11.19.42 Am)

The packaging label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, USP by AvKARE shows the 50 mg/0.2 mg strength in oral tablet form. The label highlights it is a prescription drug containing 90 tablets. The label includes drug warnings, storage instructions, barcode, and identifies AvKARE as the distributor.*

* 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.