NDC 54868-4807 Advicor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4807 - Advicor
Product Characteristics
Product Packages
NDC Code 54868-4807-0
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-4807-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-4807?
What are the uses for Advicor?
Which are Advicor UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- LOVASTATIN (UNII: 9LHU78OQFD)
- LOVASTATIN (UNII: 9LHU78OQFD) (Active Moiety)
Which are Advicor 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:
- POVIDONE (UNII: FZ989GH94E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Advicor?
- RxCUI: 582041 - 24 HR lovastatin 20 MG / niacin 1000 MG Extended Release Oral Tablet
- RxCUI: 582041 - 24 HR Lovastatin 20 MG / nicotinic acid 1000 MG Extended Release Oral Tablet
- RxCUI: 582041 - 24 HR Lovastatin 20 MG / vitamin B3 1000 MG Extended Release Oral Tablet
- RxCUI: 582041 - 24 HR Lovastatin 20 MG / vit-B3 1000 MG Extended Release Oral Tablet
- RxCUI: 582041 - lovastatin 20 MG / niacin 1000 MG 24 HR Extended Release Oral Tablet
* 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".