NDC 60760-411 Fenofibrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60760 - St. Mary's Medical Park Pharmacy
- 60760-411 - Fenofibrate
Product Characteristics
Product Packages
NDC Code 60760-411-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 60760-411?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Fenofibrate?
- RxCUI: 349287 - fenofibrate 160 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Fenofibrate
Fenofibrate is used with a low-fat diet, exercise, and sometimes with other medications to reduce the amounts of fatty substances such as cholesterol and triglycerides in the blood and to increase the amount of HDL (high-density lipoprotein; a type of fatty substance that decreases the risk of heart disease) in the blood. Build-up of cholesterol and fats along the walls of the arteries (a process known as atherosclerosis) decreases the blood flow and, therefore, the oxygen supply to the heart, brain, and other parts of the body. This increases the risk of heart disease, angina (chest pain), strokes, and heart attacks. Although fenofibrate decreases the levels of fatty substances in the blood, it has not been shown to decrease the risk of heart attacks or strokes. Fenofibrate is in a class of medications called antilipemic agents. It works by speeding the natural processes that remove cholesterol from the body.
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* Please review the disclaimer below.
[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".