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
- 11534-166_c5432731-23bc-44cf-bfcc-e59d16437db2
- Product NDC
- 11534-166
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- sodium polystyrene sulfonate
- Labeler
- SUNRISE PHARMACEUTICAL, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170124
- 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
- 15 g in 1 BOTTLE (11534-166-15) · 11534-166-15
- 15 g in 1 BOTTLE (11534-166-16) · 11534-166-16
- 454 g in 1 JAR (11534-166-44) · 11534-166-44
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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