NDC 13310-102 Fibricor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
OVAL (C48345)
19 MM
AR;788
Code Structure Chart
Product Details
What is NDC 13310-102?
What are the uses for Fibricor?
Which are Fibricor UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENOFIBRIC ACID (UNII: BGF9MN2HU1)
- FENOFIBRIC ACID (UNII: BGF9MN2HU1) (Active Moiety)
Which are Fibricor 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:
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Fibricor?
- RxCUI: 860880 - fenofibric acid 105 MG Oral Tablet
- RxCUI: 860884 - FIBRICOR 105 MG Oral Tablet
- RxCUI: 860884 - fenofibric acid 105 MG Oral Tablet [Fibricor]
- RxCUI: 860884 - Fibricor (fenofibric acid 105 MG) Oral Tablet
- RxCUI: 860884 - Fibricor 105 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".