NDC 68151-4295 Renagel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-4295 - Renagel
Product Characteristics
Product Packages
NDC Code 68151-4295-1
Package Description: 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 68151-4295?
What are the uses for Renagel?
Which are Renagel UNII Codes?
The UNII codes for the active ingredients in this product are:
- SEVELAMER HYDROCHLORIDE (UNII: GLS2PGI8QG)
- SEVELAMER (UNII: 941N5DUU5C) (Active Moiety)
Which are Renagel 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)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
What is the NDC to RxNorm Crosswalk for Renagel?
- RxCUI: 857216 - sevelamer HCl 400 MG Oral Tablet
- RxCUI: 857216 - sevelamer hydrochloride 400 MG Oral Tablet
- RxCUI: 857218 - RenaGel 400 MG Oral Tablet
- RxCUI: 857218 - sevelamer hydrochloride 400 MG Oral Tablet [RenaGel]
* 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".