NDC 54868-5526 Cholestyramine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5526 - Cholestyramine
Product Characteristics
Product Packages
NDC Code 54868-5526-0
Package Description: 60 PACKET in 1 CARTON / 5 g in 1 PACKET
Product Details
What is NDC 54868-5526?
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)
- CITRIC ACID ANHYDROUS (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)
- ASPARTAME (UNII: Z0H242BBR1)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Cholestyramine?
- RxCUI: 1801279 - cholestyramine Sugar-Free 4 GM Powder for Oral Suspension
- RxCUI: 1801279 - Sugar-Free cholestyramine resin 4000 MG Powder for Oral Suspension
- 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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[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".