Active Ingredient: SODIUM POLYSTYRENE SULFONATE
Proprietary Name: SODIUM POLYSTYRENE SULFONATE
Dosage Form; Route of Administration: POWDER; ORAL, RECTAL
Strength: 453.6GM/BOT
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A088786
Product Number: 001
Approval Date: Sep 11, 1984
Applicant Holder Full Name: PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
