NDC 68151-4718 Fenofibrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-4718 - Fenofibrate
Product Characteristics
Product Packages
NDC Code 68151-4718-9
Package Description: 1 TABLET in 1 PACKAGE
Product Details
What is NDC 68151-4718?
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)
- FENOFIBRIC ACID (UNII: BGF9MN2HU1) (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:
- TALC (UNII: 7SEV7J4R1U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- SUCROSE (UNII: C151H8M554)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CROSPOVIDONE (UNII: 68401960MK)
What is the NDC to RxNorm Crosswalk for Fenofibrate?
- RxCUI: 477562 - fenofibrate 48 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".