Cholestyramine Powder, For Suspension
Product Images NDC 33342-293

3 FDA label images from Macleods Pharmaceuticals Limited · 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 Cholestyramine (NDC 33342-293). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals Limited, 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

587 (Cholestyramine Struct)

587 (Cholestyramine Struct)
Chemical structure of Cholestyramine shown as a polymeric chain with aromatic rings and quaternary ammonium groups including trimethylammonium chloride substituents.*
FDA Label Image

569 (Cholestyramine Suspension Carton)

569 (Cholestyramine Suspension Carton)
Cholestyramine for Oral Suspension, USP powder, orange flavor, 4 grams Cholestyramine resin per pouch. The label shows a pack of 60 single dose pouches with sucrose. Manufactured by Macleods Pharmaceuticals Limited and distributed by Macleods Pharma USA, Inc. Instructions for preparation and mixing with beverages or foods are included on the label.*
FDA Label Image

565 (Cholestyramine Label)

565 (Cholestyramine Label)
Drug label for Cholestyramine for Oral Suspension, USP, 4 g/9 g powder, orange flavor. It includes dosage information, preparation instructions to mix one level scoopful with water or beverage, storage conditions, and manufacturer details for Macleods Pharmaceuticals Ltd. The label indicates 42 measured doses in a 378 g package and contains warnings about the scoop's exclusivity and sucrose content.*

* 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.