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Fosrenol
Fosrenol - 55154-5953-0 - (lanthanum carbonate)
Drug Information of Fosrenol
| 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) |
Labeler Information of Fosrenol
| 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 Information of Fosrenol
| Package NDC: | 55154-5953-0 |
| Package Description: | 10 POUCH in 1 BAG (55154-5953-0) > 1 TABLET, CHEWABLE in 1 POUCH |
NDC Information of Fosrenol
| NDC Code | 55154-5953-0 |
| Proprietary Name | Fosrenol |
| Package Description | 10 POUCH in 1 BAG (55154-5953-0) > 1 TABLET, CHEWABLE in 1 POUCH |
| 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 |
