NDC 54868-5697 Fenofibrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5697 - Fenofibrate
Product Characteristics
Product Packages
NDC Code 54868-5697-0
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5697-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5697?
What are the uses for Fenofibrate?
Which are Fenofibrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENOFIBRATE (UNII: U202363UOS)
- FENOFIBRATE (UNII: U202363UOS) (Active Moiety)
Which are Fenofibrate 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- HYPROMELLOSE 2910 (50 MPA.S) (UNII: 1IVH67816N)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Fenofibrate?
- RxCUI: 349287 - fenofibrate 160 MG Oral Tablet
- RxCUI: 351133 - fenofibrate 54 MG Oral Tablet
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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".