Fosrenol Tablet, Chewable
NDC Package 54092-252-90
Package Information
Fosrenol (lanthanum carbonate) tablets is lanthanum is used to lower high blood phosphate levels in people who are on dialysis due to severe kidney disease. This formulation utilizes a tablet, chewable delivery system. Marketed by Takeda Pharmaceuticals America, Inc., this product is identified by NDC 54092-252 and is authorized under FDA application NDA021468.
Identification & Billing
- RxCUI: 1551881 - lanthanum carbonate 1000 MG Oral Powder
- RxCUI: 1551884 - Fosrenol 1000 MG Oral Powder
- RxCUI: 1551884 - lanthanum carbonate 1000 MG Oral Powder [Fosrenol]
- RxCUI: 1551885 - lanthanum carbonate 750 MG Oral Powder
- RxCUI: 1551886 - Fosrenol 750 MG Oral Powder
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 54092 - Takeda Pharmaceuticals America, Inc.
- 54092-252 - Fosrenol
- 54092-252-90 - 2 BOTTLE in 1 PACKAGE / 45 TABLET, CHEWABLE in 1 BOTTLE (54092-252-45)
- 54092-252 - Fosrenol
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 54092-252-90 identifies a specific commercial package of 2 bottle in 1 package / 45 tablet, chewable in 1 bottle (54092-252-45) of Fosrenol, a human prescription drug labeled by Takeda Pharmaceuticals America, Inc.. This tablet, chewable is formulated for oral use and contains lanthanum carbonate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Takeda Pharmaceuticals America, Inc. on October 26, 2004. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Lanthanum is used to lower high blood phosphate levels in people who are on dialysis due to severe kidney disease. Dialysis removes some phosphate from your blood, but it is difficult to remove enough to keep your phosphate levels balanced. Decreasing blood phosphate levels can help keep your bones strong, prevent unsafe buildup of minerals in your body, and may decrease the risk of heart disease and strokes that can result from high phosphate levels. Lanthanum is a natural mineral that works by binding to phosphate in the foods you eat. The phosphate then passes out of your body in your stool.
How is this Takeda Pharmaceuticals America, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 54092025290. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 2 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.