# Sodium Polystyrene Sulfonate

NDC: 10702-036
Generic name: Sodium Polystyrene Sulfonate
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: ORAL, RECTAL
Marketing started: 20120725

FDA application: ANDA040905

## Active ingredients

- SODIUM POLYSTYRENE SULFONATE: 1 g/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10702-036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=905c3ee5-d1a7-4deb-a345-4a42296704fa