NDC 17856-0021 Renagel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0021 - Renagel
Product Characteristics
Product Packages
NDC Code 17856-0021-2
Package Description: 1 TABLET in 1 POUCH
Product Details
What is NDC 17856-0021?
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: 857224 - sevelamer HCl 800 MG Oral Tablet
- RxCUI: 857224 - sevelamer hydrochloride 800 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Sevelamer
Sevelamer is used to control high blood levels of phosphorus in people with chronic kidney disease who are on dialysis (medical treatment to clean the blood when the kidneys are not working properly). Sevelamer is in a class of medications called phosphate binders. It binds phosphorus that you get from foods in your diet and prevents it from being absorbed into your blood stream.
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* 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".