Renagel - 58468-0021-3 - (Renagel)

Alphabetical Index


Drug Information of Renagel

Product NDC: 58468-0021
Proprietary Name: Renagel
Non Proprietary Name: Renagel
Active Ingredient(s): 800    mg/1 & nbsp;   Renagel
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Renagel

Product NDC: 58468-0021
Labeler Name: Genzyme Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021179
Marketing Category: NDA
Start Marketing Date: 20080606

Package Information of Renagel

Package NDC: 58468-0021-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (58468-0021-3)

NDC Information of Renagel

NDC Code 58468-0021-3
Proprietary Name Renagel
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (58468-0021-3)
Product NDC 58468-0021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Renagel
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080606
Marketing Category Name NDA
Labeler Name Genzyme Corporation
Substance Name SEVELAMER HYDROCHLORIDE
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]

Complete Information of Renagel


General Information