NDC 72162-1230
Sodium Polystyrene Sulfonate 4.1 meq per 1 g powder, for suspension
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Sunrise Pharmaceutical, Inc.'s NDC 11534-166.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sunrise Pharmaceutical Inc | Rahway, NJ, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 31, 2026 · 8 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Polystyrene Sulfonic Acid: every company that makes it
- Form
- powder, for suspension, oral; rectal
- Strength
- 4.1 meq per 1 g
- Approval
- ANDA ANDA204071
- On the market since
- Jan 24, 2017
- Package NDCs
72162-1230-272162-1230-7- Official label
- DailyMed (National Library of Medicine), updated May 12, 2025
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