United States · FDA National Drug Code directory
Sodium Polystyrene Sulfonate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 24658-760_ae811fb8-9a78-496f-b710-663bc678f8e7
- Product NDC
- 24658-760
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- Sodium Polystyrene Sulfonate
- Labeler
- PuraCap Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161215
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM POLYSTYRENE SULFONATE — 4.1 meq/g
These values do not establish equivalence or a dose recommendation.
Packages
- 453.6 g in 1 JAR (24658-760-16) · 24658-760-16
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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