Strength
1 g/g
Manufacturer
CMP Pharma, Inc.NDC
46287001216
Classification
Generic
Dosage Form
POWDER, FOR SUSPENSION
Route
ORAL; RECTAL
Last Updated
4/22/2026
Active Ingredients
SODIUM POLYSTYRENE SULFONATEApproval Type
Generic (ANDA)
FDA Application
ANDA089910On Market Since
1/19/1989
Related Drugs
Same classification
No related drugs found.