Cholestyramine Light 01
Cholestyramine Light Powder, For Suspension
Product Images NDC 51224-009
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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cholestyramine Light (NDC 51224-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Tagi Pharma, 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.
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Cholestyramine Light 02
This is a description of a medication called "Cholestyramine for Oral Suspension USP, Light". It is supplied in single-dose pouches, with 4 grams of cholestyramine resin USP in each pouch. The medication needs to be mixed with water or any noncarbonated beverage before use. It can be mixed and refrigerated for three days. The dosage must be as directed in the accompanying literature, and it is important to maintain a proper diet and exercise routine. The medication contains an artificial sweetener, Aspartame. There are some warnings mentioned in the text, including one stating that the package is not child-resistant and should be kept out of reach of children. The name of the manufacturers of the medication is mentioned as well.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
