Diclofenac Sodium And Misoprostol Tablet, Delayed Release
Product Images NDC 65162-438

2 FDA label images from Amneal Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

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 65162-438). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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.

Product Images & Figures Index

FDA Label Image

50 mg Label (Diclofenac Sodium And Misoprostol Delayed Release 1)

50 mg Label (Diclofenac Sodium And Misoprostol Delayed Release 1)
Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, USP, 50 mg/200 mcg, oral delayed-release tablets. The label indicates a package of 100 tablets with a prescription-only designation. It includes dosage form, strengths, directions for pharmacists, storage conditions, manufacturer Amneal Pharmaceuticals LLC in Bridgewater, NJ, and warning information highlighted in red about contraindications for pregnant women. The label also features a QR code and barcode.*
FDA Label Image

75 mg Label (Diclofenac Sodium And Misoprostol Delayed Release 2)

75 mg Label (Diclofenac Sodium And Misoprostol Delayed Release 2)
Label for Diclofenac Sodium and Misoprostol Delayed-Release Tablets, USP 75 mg/200 mcg by Amneal Pharmaceuticals LLC. The label indicates a prescription-only oral delayed-release tablet with 100 tablets per container. Storage instructions and a QR code for the medication guide are included, along with warnings and pharmacist dispensing information.*

* 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.