Cholestyramine Powder, For Suspension
Product Images NDC 68382-529

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 68382-529). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (usa) 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

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Chemical structure diagram representing the main polymeric groups of cholestyramine, the active ingredient in the product. The structure includes aromatic rings and quaternary ammonium groups, highlighting the polymeric nature of cholestyramine used in oral suspension form.*

FDA Label Image

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This drug facts panel for Cholestyramine for Oral Suspension USP, Light Powder, 4 grams per scoop, provides preparation instructions for mixing the powder with water or a noncarbonated beverage. It includes dosage information, warnings for phenylketonurics, storage instructions, and manufacturer details (Cadila Healthcare Ltd. and Zydus Pharmaceuticals USA Inc.). The label also mentions the orange vanilla flavor, container contents, and barcode.*

FDA Label Image

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Cholestyramine for Oral Suspension USP, Light Powder 4 g/5.5 g pouch, orange vanilla flavor, packaged in 60 single-dose pouches. The label states it is for oral suspension use and includes preparation instructions with images for mixing with fluids like applesauce or beverages. The labeler is Zydus Pharmaceuticals (USA) Inc. and it displays the NDC 68382-529-60 and an Rx only symbol.*

* 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.