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Sodium Polystyrene Sulfonate

NDC 10702-036 · HUMAN PRESCRIPTION DRUG · POWDER

Labeler / ManufacturerKVK-Tech, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040905
Dosage form / routePOWDER · ORAL RECTAL
Active ingredientsSODIUM POLYSTYRENE SULFONATE (1 g/g)
Marketing started20120725
Package count2

External sources

Source: openFDA. Public-domain (CC0).