Sulfasalazine Tablet
Product Images NDC 11534-200

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sulfasalazine (NDC 11534-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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

Principal Display Panel (500 mg Tablet Bottle Label)

Label for Sulfasalazine Tablets, USP 500 mg oral tablets manufactured by Sunrise Pharmaceutical, Inc. The label indicates the product contains 100 tablets in a bulk container, with storage instructions and a barcode visible. The NDC is 11534-200-01 and the label is dated Rev. 12/2022.*

FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Label for Sulfasalazine Tablets, USP 500 mg oral tablets in a bulk container of 300 tablets. The product is manufactured for Sunrise Pharmaceutical, Inc. The label includes storage instructions, dosage note referring to prescribing information, and a barcode. The label states Rx Only and provides temperature storage guidelines.*

FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Label for Sulfasalazine Tablets USP 500 mg oral tablets. The label indicates the package contains 500 tablets and is manufactured for Sunrise Pharmaceutical, Inc., Rahway, NJ. It includes dosage strength, barcode, storage instructions, and NDC 11534-200-04 with Rx Only status.*

FDA Label Image

Chemical Structure (Chemical Structure)

Chemical structure diagram of Sulfasalazine showing its molecular arrangement, including benzene rings, azo group, sulfonamide, and carboxylic acid functional groups.*

* 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.