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  5. NDC Package Code: 62559-356-01 Kionex

NDC Package 62559-356-01 Kionex

Sodium Polystyrene Sulfonate Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
62559-356-01
Package Description:
10 BOTTLE in 1 CASE / 60 mL in 1 BOTTLE (62559-356-60)
Product Code:
62559-356
Proprietary Name:
Kionex
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:
62559035601
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • 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
  • RxCUI: 793741 - Kionex 15 GM in 60 mL Oral or Rectal Suspension
Product Type:
Human Prescription Drug
Labeler Name:
Ani Pharmaceuticals, Inc.
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
SODIUM POLYSTYRENE SULFONATE 15 g/60mL
Sample Package:
No
FDA Application Number:
ANDA040028
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
05-03-2024
Listing Expiration Date:
12-31-2026
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 62559-356-01?

The NDC Packaged Code 62559-356-01 is assigned to a package of 10 bottle in 1 case / 60 ml in 1 bottle (62559-356-60) of Kionex, a human prescription drug labeled by Ani Pharmaceuticals, Inc.. The product's dosage form is suspension and is administered via oral form.

Is NDC 62559-356 included in the NDC Directory?

Yes, Kionex with product code 62559-356 is active and included in the NDC Directory. The product was first marketed by Ani Pharmaceuticals, Inc. on May 03, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 62559-356-01?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 62559-356-01?

The 11-digit format is 62559035601. 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 5-3-2 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
5-3-262559-356-015-4-262559-0356-01