Sulindac Tablet
Product Images NDC 24658-770

3 FDA label images from Puracap Laboratories Llc Dba Blu Pharmaceuticals · 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 Sulindac (NDC 24658-770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puracap Laboratories Llc Dba Blu Pharmaceuticals, 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

Structure Formula

Structure Formula
Chemical structure diagram showing the conversion of Sulindac through its metabolites: sulindac (sulfide), sulindac (sulfoxide), and sulindac (sulfone). The image illustrates the molecular changes and intermediate forms of the active ingredient Sulindac.*
FDA Label Image

Sulindac 150mg 100ct

Sulindac 150mg 100ct
Label for Sulindac Tablets, USP 150 mg oral tablets in a pack of 100 by PuraCap Laboratories LLC dba Blu Pharmaceuticals. The label includes dosage strength, NDC code 24658-770-01, storage guidelines, dispensing instructions, and warnings to keep out of reach of children. It displays the American flag and states the product is manufactured in the USA.*
FDA Label Image

Sulindac 200mg 500ct

Sulindac 200mg 500ct
The label for Sulindac Tablets, USP features a strength of 200 mg and indicates an oral tablet dosage form. The product is prescription-only and packaged as 500 tablets. The label includes storage instructions, dosage warnings, and states the distributor as PuraCap Laboratories LLC operating as Blu Pharmaceuticals in Franklin, KY. A barcode and manufacturing origin (USA) are also present.*

* 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.