Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 43063-467

3 FDA label images from Pd-rx Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 43063-467). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

43063467 Label (43063467)

43063467 Label (43063467)
Label for Diclofenac Sodium delayed release tablets, 50 mg strength, packaged with 30 tablets. The label shows the product NDC 43063-467-30 and the manufacturer as PD-Rx Pharmaceuticals, Inc. It includes warnings to keep out of reach of children and not to consume alcohol with this medication. The lot number is F21D02 and expiration date is 06/2023. Directions mention taking the tablets with food.*
FDA Label Image

1 (Image 1)

1 (Image 1)
Chemical structure diagram of Diclofenac Sodium showing the molecular arrangement including chlorinated aromatic rings, an amine group, a carboxylate group, and a sodium ion.*
FDA Label Image

1 (Image 2)

1 (Image 2)
Diclofenac Sodium 50 mg delayed release oral tablets carton and bottle label from PD-Rx Pharmaceuticals, Inc. The packaging shows the product name, strength, dosage form, and labeler prominently with the NDC 43063-467. The label includes standard regulatory and usage information panels.*

* 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.