NDC 50090-3415 Cholestyramine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 50090-3415?
What are the uses for Cholestyramine?
Which are Cholestyramine UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHOLESTYRAMINE (UNII: 4B33BGI082)
- CHOLESTYRAMINE (UNII: 4B33BGI082) (Active Moiety)
Which are Cholestyramine Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ACACIA (UNII: 5C5403N26O)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL ALGINATE (UNII: 26CD3J2R0C)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Cholestyramine?
- RxCUI: 848943 - cholestyramine resin 4 GM Powder for Oral Suspension
- RxCUI: 848943 - cholestyramine resin 4000 MG Powder for Oral Suspension
- RxCUI: 848943 - cholestyramine resin 4 GM per 9 GM Powder for Oral Suspension
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Patient Education
Cholestyramine Resin
Cholestyramine is used with diet changes (restriction of cholesterol and fat intake) to reduce the amount of cholesterol and certain fatty substances in your blood. Accumulation of cholesterol and fats along the walls of your arteries (a process known as atherosclerosis) decreases blood flow and, therefore, the oxygen supply to your heart, brain, and other parts of your body. Lowering your blood level of cholesterol and fats may help to prevent heart disease, angina (chest pain), strokes, and heart attacks. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".