NDC 52725-495 Fenoglide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
18 MM
FHI
Code Structure Chart
Product Details
What is NDC 52725-495?
What are the uses for Fenoglide?
Which are Fenoglide UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENOFIBRATE (UNII: U202363UOS)
- FENOFIBRATE (UNII: U202363UOS) (Active Moiety)
Which are Fenoglide 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Fenoglide?
- RxCUI: 749802 - fenofibrate 120 MG Oral Tablet
- RxCUI: 749804 - fenofibrate 40 MG Oral Tablet
- RxCUI: 763250 - Fenoglide 120 MG Oral Tablet
- RxCUI: 763250 - fenofibrate 120 MG Oral Tablet [Fenoglide]
- RxCUI: 763252 - Fenoglide 40 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".