Cholestyramine Powder, For Suspension
Product Images NDC 27241-134

3 FDA label images from Ajanta Pharma Usa Inc. · 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 27241-134). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ajanta Pharma 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.

Product Images & Figures Index

FDA Label Image

Cholestyramine (Cholestyramine)

Cholestyramine (Cholestyramine)
Chemical structure diagram of the active ingredient Cholestyramine, showing repeating aromatic rings with attached side groups including a quaternary ammonium chloride group.*
FDA Label Image

Cholestyramine9g

Cholestyramine9g
Cholestyramine for Oral Suspension USP powder, 4 g per 9 g sachet, orange flavor. The single-dose sachet is marketed by Ajanta Pharma USA Inc. The label includes preparation instructions to mix the powder with 2 to 6 ounces of water or beverage, storage conditions, and warnings that the sachet is not child-resistant and contains sucrose.*
FDA Label Image

Cholestyramine_378g (Cholestyramine 378g)

Cholestyramine_378g (Cholestyramine 378g)
This text panel contains preparation instructions, dosage information, and storage guidelines for Cholestyramine for Oral Suspension, USP Powder. It specifies the scoop size, mixing directions, usual dosage, and cautions about child safety and storage temperatures. It also notes the package contains 378 g total with 168 g of Cholestyramine resin and is orange flavored. Manufacturer details for Ajanta Pharma USA Inc. are included.*

* 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.