NDC 11534-166
Sodium Polystyrene Sulfonate 4.1 meq per 1 g powder, for suspension
On the label: Sunrise Pharmaceutical, Inc..
Where it's 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 |
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
11534-166-1511534-166-1611534-166-44- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?