Sodium Polystyrene Sulfonate Suspension
NDC Package 46287-006-01
Package Information
Sodium Polystyrene Sulfonate suspension is a medication used to treat a high level of potassium in your blood. This formulation utilizes a suspension delivery system. Marketed by Cmp Pharma, Inc., this product is identified by NDC 46287-006 and is authorized under FDA application ANDA087859.
Identification & Billing
- RxCUI: 313072 - sodium polystyrene sulfonate 15 GM in 60 mL Oral or Rectal Suspension
- RxCUI: 313072 - sodium polystyrene sulfonate 250 MG/ML Oral Suspension
- RxCUI: 313072 - sodium polystyrene sulfonate 15 GM per 60 ML Oral Suspension
- RxCUI: 313072 - sodium polystyrene sulfonate 30 GM per 120 ML Oral Suspension
Clinical Specifications
- Oral - Administration to or by way of the mouth.
- Rectal - Administration to the rectum.
Regulatory & Marketing
Hierarchy Structure
- 46287 - Cmp Pharma, Inc.
- 46287-006 - Sodium Polystyrene Sulfonate
- 46287-006-01 - 473 mL in 1 BOTTLE
- 46287-006 - Sodium Polystyrene Sulfonate
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.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (46287-006). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 46287-006-01 identifies a specific commercial package of 473 ml in 1 bottle of Sodium Polystyrene Sulfonate, a human prescription drug labeled by Cmp Pharma, Inc.. This suspension is formulated for oral; rectal use and contains sodium polystyrene sulfonate 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 Cmp Pharma, Inc. on December 08, 1982. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is used to treat a high level of potassium in your blood. Too much potassium in your blood can sometimes cause heart rhythm problems. Sodium polystyrene sulfonate works by helping your body get rid of extra potassium.
How is this Cmp Pharma, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 46287000601. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 473 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.