# Sodium Polystyrene Sulfonate

NDC: 17856-0024
Generic name: Sodium Polystyrene Sulfonate
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20140414

FDA application: ANDA202333

## Active ingredients

- SODIUM POLYSTYRENE SULFONATE: 4.1 meq/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d95d23e-94c8-4975-99f5-ce746dfbb60e