Cholestyramine Powder, For Suspension
Product Images NDC 68382-528

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 68382-528). 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 of cholestyramine polymeric groups showing repeating styrene and quaternary ammonium chloride units, representing the main polymeric groups of the active ingredient.*

FDA Label Image

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Label for Cholestyramine for Oral Suspension USP Powder, 4 grams of cholestyramine resin per scoopful, orange vanilla flavor. The powder is provided in a 378-gram container with 42 measured doses. Manufactured by Cadila Healthcare Ltd., India, and distributed by Zydus Pharmaceuticals (USA) Inc. The label includes preparation instructions, storage conditions, and child safety warnings.*

FDA Label Image

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The packaging label for Cholestyramine powder for oral suspension by Zydus Pharmaceuticals (USA) Inc. shows the product name and strength of 4 grams. It includes preparation instructions with images, indicating mixing with foods or beverages. The label states orange vanilla flavor and notes the presence of sucrose. The package contains 60 single dose pouches, NDC 68382-528-60.*

* 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.