# Sodium Polystyrene Sulfonate

NDC: 46287-012
Generic name: Sodium Polystyrene Sulfonate
Labeler / Manufacturer: CMP Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL, RECTAL
Marketing started: 19890119

FDA application: ANDA089910

## 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:"46287-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46287-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2017bfbe-cda8-46f1-b4f1-9c086c3249a9