Product NDC: | 0179-0043 |
Proprietary Name: | Renvela |
Non Proprietary Name: | SEVELAMER CARBONATE |
Active Ingredient(s): | 800 mg/1 & nbsp; SEVELAMER CARBONATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0179-0043 |
Labeler Name: | KAISER FOUNDATION HOSPITALS |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022127 |
Marketing Category: | NDA |
Start Marketing Date: | 20100212 |
Package NDC: | 0179-0043-70 |
Package Description: | 30 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0179-0043-70) |
NDC Code | 0179-0043-70 |
Proprietary Name | Renvela |
Package Description | 30 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0179-0043-70) |
Product NDC | 0179-0043 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SEVELAMER CARBONATE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100212 |
Marketing Category Name | NDA |
Labeler Name | KAISER FOUNDATION HOSPITALS |
Substance Name | SEVELAMER CARBONATE |
Strength Number | 800 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |