Kionex - 0574-2002-16 - (Sodium Polystyrene Sulfonate)

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Drug Information of Kionex

Product NDC: 0574-2002
Proprietary Name: Kionex
Non Proprietary Name: Sodium Polystyrene Sulfonate
Active Ingredient(s): 15    g/60mL & nbsp;   Sodium Polystyrene Sulfonate
Administration Route(s): ORAL; RECTAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Kionex

Product NDC: 0574-2002
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040028
Marketing Category: ANDA
Start Marketing Date: 20081230

Package Information of Kionex

Package NDC: 0574-2002-16
Package Description: 473 mL in 1 BOTTLE (0574-2002-16)

NDC Information of Kionex

NDC Code 0574-2002-16
Proprietary Name Kionex
Package Description 473 mL in 1 BOTTLE (0574-2002-16)
Product NDC 0574-2002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Polystyrene Sulfonate
Dosage Form Name SUSPENSION
Route Name ORAL; RECTAL
Start Marketing Date 20081230
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, LLC
Substance Name SODIUM POLYSTYRENE SULFONATE
Strength Number 15
Strength Unit g/60mL
Pharmaceutical Classes

Complete Information of Kionex


General Information