Kionex - 0574-2004-16 - (SODIUM POLYSTYRENE SULFONATE)

Alphabetical Index


Drug Information of Kionex

Product NDC: 0574-2004
Proprietary Name: Kionex
Non Proprietary Name: SODIUM POLYSTYRENE SULFONATE
Active Ingredient(s): 4.1    meq/g & nbsp;   SODIUM POLYSTYRENE SULFONATE
Administration Route(s): ORAL; RECTAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Kionex

Product NDC: 0574-2004
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040029
Marketing Category: ANDA
Start Marketing Date: 19980201

Package Information of Kionex

Package NDC: 0574-2004-16
Package Description: 454 g in 1 BOTTLE, PLASTIC (0574-2004-16)

NDC Information of Kionex

NDC Code 0574-2004-16
Proprietary Name Kionex
Package Description 454 g in 1 BOTTLE, PLASTIC (0574-2004-16)
Product NDC 0574-2004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM POLYSTYRENE SULFONATE
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL; RECTAL
Start Marketing Date 19980201
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, LLC
Substance Name SODIUM POLYSTYRENE SULFONATE
Strength Number 4.1
Strength Unit meq/g
Pharmaceutical Classes

Complete Information of Kionex


General Information