NDC 68151-4068 Niaspan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-4068 - Niaspan
Product Characteristics
Product Packages
NDC Code 68151-4068-9
Package Description: 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE
Product Details
What is NDC 68151-4068?
What are the uses for Niaspan?
Which are Niaspan UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
Which are Niaspan 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:
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POVIDONES (UNII: FZ989GH94E)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
What is the NDC to RxNorm Crosswalk for Niaspan?
- RxCUI: 1098141 - niacin 500 MG 24HR Extended Release Oral Tablet
- RxCUI: 1098141 - 24 HR niacin 500 MG Extended Release Oral Tablet
- RxCUI: 1098141 - 24 HR nicotinic acid 500 MG Extended Release Oral Tablet
- RxCUI: 1098141 - 24 HR vitamin B3 500 MG Extended Release Oral Tablet
- RxCUI: 1098141 - 24 HR vit-B3 500 MG 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".