NDC 17856-0036
Sodium Polystyrene Sulfonate 1 g per 1 g powder
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from KVK-TECH, Inc.'s NDC 10702-036.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it and relabels it
Product details
- Generic drug
- Polystyrene Sulfonic Acid: every company that makes it
- Form
- powder
- Strength
- 1 g per 1 g
- Approval
- ANDA ANDA040905
- On the market since
- Jul 25, 2012
- Package NDCs
17856-0036-1- Official label
- DailyMed (National Library of Medicine), updated May 4, 2016
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