Active Ingredient: SODIUM POLYSTYRENE SULFONATE
Proprietary Name: KIONEX
Dosage Form; Route of Administration: POWDER; ORAL, RECTAL
Strength: 454GM/BOT
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A040029
Product Number: 001
Approval Date: Feb 6, 1998
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information