Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 51407-967

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 51407-967). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-536-01lb (Diclofenac Sodium 25 mg)

Label for Diclofenac Sodium Delayed-Release Tablets USP, 25 mg, showing the NDC 51407-536-01. The label indicates 100 oral tablets, with instructions for dispensing and storage, including protection from moisture and temperature control. The labeler is Golden State Medical Supply, Inc., and it includes barcodes and a note for pharmacists to provide medication guides to patients.*

FDA Label Image

51407-967-01lb (Diclofenac Sodium 50 mg)

Label for Diclofenac Sodium Delayed-Release Tablets USP 50 mg oral tablets. The label shows a package of 100 tablets, Rx only, marketed by GSMS Incorporated. The NDC number is 51407-967-01. Storage instructions, usage directions, and warnings to keep out of reach of children and protect from moisture are included.*

FDA Label Image

51407-968-01lb (Diclofenac Sodium 75 mg)

Label for Diclofenac Sodium Delayed Release Tablets USP 75 mg by Golden State Medical Supply, Inc. The label shows 100 tablets, oral delayed-release form, with the active ingredient strength clearly stated. It includes dosage form, manufacturer details, storage instructions, and barcode.*

FDA Label Image

Figure (Dic05 0006 01)

Chemical structure of Diclofenac Sodium, showing two chlorinated aromatic rings connected via an amine group, with a carboxylate sodium salt group.*

* 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.