Balsalazide Disodium Capsule
Product Images NDC 72789-149

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 Balsalazide Disodium (NDC 72789-149). 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Balsalazide Chem)

Chemical Structure (Balsalazide Chem)
Chemical structure diagram of Balsalazide Disodium, displaying the molecular framework with sodium carboxylate groups, azo linkage, aromatic rings, and hydrated form with two water molecules.*
FDA Label Image

Figure 1 (Balsalazide Fig 1)

Figure 1 (Balsalazide Fig 1)
A bar graph depicting the percentage of patients improved based on stool blood, stool frequency, and sigmoidoscopy results for two doses of Balsalazide Disodium: 2.25 g (0.8 g mesalamine equivalents) and 6.75 g (2.4 g mesalamine equivalents). The higher dose shows greater improvement percentages in all categories, with p-values indicating statistical significance.*
FDA Label Image

72789149 Label (72789149)

72789149 Label (72789149)
Balsalazide Disodium USP 750 mg oral capsules label showing a package size of 280 capsules. The label includes storage instructions, a barcode, and contact information for PD-Rx Pharmaceuticals, Inc. in Oklahoma City, OK, and the manufacturer West-Ward Pharmaceuticals in Columbus, Ohio. The label also displays the product NDC 72789-149-69 and indicates the product is Rx only.*

* 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.