Cholestyramine Powder, For Suspension
Product Images NDC 70771-1070

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 70771-1070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

Formula (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 01)

Chemical structure diagram showing the main polymeric groups of cholestyramine, including aromatic rings and associated functional groups, as represented in the polymer.*

FDA Label Image

Label (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 02)

Label for Cholestyramine for Oral Suspension USP, Light Powder, 4 grams cholestyramine resin per scoopful, orange vanilla flavor. The label indicates prescription use only, contains 231 g total with 42 measured doses. Manufactured by Cadila Healthcare Ltd., Baddi, India, under Zydus Lifesciences Limited. Preparation instructions explain mixing powder with water or beverage before use, with warning for phenylketonurics regarding phenylalanine content. Storage instructions and usual dosage advisories are included.*

FDA Label Image

Carton (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 03)

Packaging label for Cholestyramine for Oral Suspension USP, Light Powder, 4 g/5.5 g strength. The label shows 60 single dose pouches of orange vanilla flavor, labeled for prescription use (Rx only). It includes preparation instructions and emphasizes mixing the powder with noncarbonated beverages. The labeler is Zydus Lifesciences Limited, with branding from ZyGenerics and NutraSweet. The product NDC is 70771-1070-2.*

* 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.