Product NDC: | 55154-5953 |
Proprietary Name: | Fosrenol |
Non Proprietary Name: | lanthanum carbonate |
Active Ingredient(s): | 500 mg/1 & nbsp; lanthanum carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-5953 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021468 |
Marketing Category: | NDA |
Start Marketing Date: | 20041026 |
Package NDC: | 55154-5953-4 |
Package Description: | 90 POUCH in 1 CARTON (55154-5953-4) > 1 TABLET, CHEWABLE in 1 POUCH (55154-5953-6) |
NDC Code | 55154-5953-4 |
Proprietary Name | Fosrenol |
Package Description | 90 POUCH in 1 CARTON (55154-5953-4) > 1 TABLET, CHEWABLE in 1 POUCH (55154-5953-6) |
Product NDC | 55154-5953 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | lanthanum carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20041026 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | LANTHANUM CARBONATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |