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
- 10702-036_1213e349-d5ef-2221-e063-6294a90a8e83
- Product NDC
- 10702-036
- Form
- POWDER
- Composition / generic term
- Sodium Polystyrene Sulfonate
- Labeler
- KVK-Tech, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120725
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM POLYSTYRENE SULFONATE — 1 g/g
These values do not establish equivalence or a dose recommendation.
Packages
- 15 g in 1 BOTTLE (10702-036-15) · 10702-036-15
- 454 g in 1 JAR (10702-036-45) · 10702-036-45
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →