NDC Package 63629-2390-1 Sodium Polystyrene Sulfonate

Powder, For Suspension Oral; Rectal - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
63629-2390-1
Package Description:
454 g in 1 JAR
Product Code:
Proprietary Name:
Sodium Polystyrene Sulfonate
Non-Proprietary Name:
Sodium Polystyrene Sulfonate
Substance Name:
Sodium Polystyrene Sulfonate
Usage Information:
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.
11-Digit NDC Billing Format:
63629239001
Billing Unit:
C48332
NDC to RxNorm Crosswalk:
  • RxCUI: 2101899 - sodium polystyrene sulfonate 15 GM Powder for Suspension
  • RxCUI: 2101899 - sodium polystyrene sulfonate 15000 MG Powder for Oral Suspension
  • RxCUI: 2101899 - sodium polystyrene sulfonate 15 to 60 GM Powder for Oral Suspension
  • RxCUI: 2101899 - sodium polystyrene sulfonate 30 to 50 GM Powder for Rectal Suspension
  • RxCUI: 2101899 - sodium polystyrene sulfonate 4.1 MEQ in 1 GM Powder for Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bryant Ranch Prepack
    Dosage Form:
    Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Rectal - Administration to the rectum.
  • Sample Package:
    No
    FDA Application Number:
    ANDA204071
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-24-2017
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 63629-2390-1?

    The NDC Packaged Code 63629-2390-1 is assigned to a package of 454 g in 1 jar of Sodium Polystyrene Sulfonate, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is powder, for suspension and is administered via oral; rectal form.

    Is NDC 63629-2390 included in the NDC Directory?

    Yes, Sodium Polystyrene Sulfonate with product code 63629-2390 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on January 24, 2017 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 63629-2390-1?

    The contents of this package are billed C48332

    What is the 11-digit format for NDC 63629-2390-1?

    The 11-digit format is 63629239001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-163629-2390-15-4-263629-2390-01