NDC 70166-712
Sodium Polystyrene Sulfonate 4.1 meq per 1 g powder, for suspension
On the label: Lohxa. It's repackaged from NDC 51293-831, made by ECI Pharmaceuticals, LLC (Sodium Polystyrene Sulfonate). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lohxa names for other drugs.
Product details
- Generic drug
- Polystyrene Sulfonic Acid: every company that makes it
- Form
- powder, for suspension
- Strength
- 4.1 meq per 1 g
- Approval
- ANDA ANDA090313
- On the market since
- Feb 7, 2017
- Package NDCs
70166-712-10- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2019
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