Cholestyramine Powder, For Suspension
Product Images NDC 33342-319

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 33342-319). 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

Structure (Cholestyramine Structure)

Structure (Cholestyramine Structure)
Chemical structure of the active ingredient Cholestyramine, depicting its polymeric form with benzene rings and quaternary ammonium groups as part of the polymer chain.*
FDA Label Image

111 (Cholestyramine Suspension Light 42 Pouches)

111 (Cholestyramine Suspension Light 42 Pouches)
Label for Cholestyramine for Oral Suspension USP, Light resin USP, 4 grams per pouch, Orange Flavor. The label includes the proprietary and generic names, strength, dosage form as powder for suspension, manufacturer Macleods Pharmaceuticals Limited, and the NDC 33342-319-72. The label also shows instructions and warning sections as part of the carton artwork.*
FDA Label Image

444 (Cholestyramine Suspension Light 60 Pouches)

444 (Cholestyramine Suspension Light 60 Pouches)
Packaging label for Cholestyramine for Oral Suspension USP, Light 4 grams per pouch by Macleods Pharmaceuticals Limited. The label indicates an orange flavor with 60 single-dose pouches. It includes product usage instructions and warnings, as well as a standardized design with green and red text elements and a barcode.*
FDA Label Image

776 (Cholestyramine Suspension Light Foil)

776 (Cholestyramine Suspension Light Foil)
Label for Cholestyramine for Oral Suspension USP, Light, 4 grams per pouch, powder for suspension, orange flavor. The single-dose pouch is labeled by Macleods Pharmaceuticals Limited with NDC 33342-319-01, marked for Rx use only. The label includes directions to open, flavor info, and manufacturer details.*

* 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.