NDC 17856-0036 Sodium Polystyrene Sulfonate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0036 - Sodium Polystyrene Sulfonate
Product Characteristics
Product Packages
NDC Code 17856-0036-1
Package Description: 15 g in 1 POUCH
Product Details
What is NDC 17856-0036?
What are the uses for Sodium Polystyrene Sulfonate?
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?
- 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
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[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".