NDC 51293-831 Sodium Polystyrene Sulfonate

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51293-831
Proprietary Name:
Sodium Polystyrene Sulfonate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eci Pharmaceuticals, Llc
Labeler Code:
51293
Start Marketing Date: [9]
02-07-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - CREAM TO LIGHT BROWN)

Product Packages

NDC Code 51293-831-97

Package Description: 453.6 g in 1 JAR

Price per Unit: $0.16767 per GM

Product Details

What is NDC 51293-831?

The NDC code 51293-831 is assigned by the FDA to the product Sodium Polystyrene Sulfonate which is product labeled by Eci Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51293-831-97 453.6 g in 1 jar . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sodium Polystyrene Sulfonate?

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.

Which are Sodium Polystyrene Sulfonate UNII Codes?

The UNII codes for the active ingredients in this product are:

  • SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
  • POLYSTYRENE SULFONIC ACID (UNII: 70KO0R01RY) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Sodium Polystyrene Sulfonate?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".