Sodium Polystyrene Sulfonate

FDA Approved: * September 11, 1984
Pharm Company: * MORTON GROVE
Category: Potassium Levels

Polystyrene sulfonates are a group of medications used to treat high blood potassium.[1] Effects generally take hours to days.[1] They are also used to remove potassium, calcium, and sodium from solutions in technical applications. Common side effects include loss of appetite, gastrointestinal upset, constipation, and low blood calcium.[1] These polymers are derived from polystyrene by the addition of sulfonate functional groups. Sodium polystyr... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
1 Discussion

Dosage List

Sodium Polystyrene Sulfonate 15 g/60ml Oral; Rectal Suspension
NDC: 0054-0379
Labeler:
Roxane Laboratories, Inc.
Sodium Polystyrene Sulfonate 15 g/60ml Oral; Rectal Suspension
NDC: 0574-2003
Labeler:
Paddock Laboratories, LLC
Sodium Polystyrene Sulfonate 1 g/g Oral Powder
NDC: 0904-6041
Labeler:
Major Pharmaceuticals
Sodium Polystyrene Sulfonate 4.1 Meq/G Oral; Rectal Powder, for Suspension
NDC: 10135-146
Labeler:
Marlex Pharmaceuticals Inc
Sodium Polystyrene Sulfonate 1 g/g Oral; Rectal Powder
NDC: 10702-036
Labeler:
Kvk-tech, Inc.
Sodium Polystyrene Sulfonate 4.1 Meq/G Oral; Rectal Powder, for Suspension
NDC: 11534-166
Labeler:
Sunrise Pharmaceutical, Inc.
Sodium Polystyrene Sulfonate 4.1 Meq/G Oral; Rectal Suspension
NDC: 13811-656
Labeler:
Trigen Laboratories, LLC
Sodium Polystyrene Sulfonate 4.1 Meq/G Oral Powder, for Suspension
NDC: 17856-0024
Labeler:
Atlantic Biologicals Corp.
Sodium Polystyrene Sulfonate 1 g/g Oral; Rectal Powder
NDC: 17856-0036
Labeler:
Atlantic Biologicals Corps
Sodium Polystyrene Sulfonate 4.1 Meq/G Oral; Rectal Powder, for Suspension
NDC: 17856-0831
Labeler:
Atlantic Biologicals Corp.
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