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Sodium Polystyrene Sulfonate - 0574-2003-16 - (Sodium Polystyrene Sulfonate)

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Drug Information of Sodium Polystyrene Sulfonate

Product NDC: 0574-2003
Proprietary Name: Sodium Polystyrene Sulfonate
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 Sodium Polystyrene Sulfonate

Product NDC: 0574-2003
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090590
Marketing Category: ANDA
Start Marketing Date: 20110921

Package Information of Sodium Polystyrene Sulfonate

Package NDC: 0574-2003-16
Package Description: 480 mL in 1 BOTTLE (0574-2003-16)

NDC Information of Sodium Polystyrene Sulfonate

NDC Code 0574-2003-16
Proprietary Name Sodium Polystyrene Sulfonate
Package Description 480 mL in 1 BOTTLE (0574-2003-16)
Product NDC 0574-2003
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Polystyrene Sulfonate
Dosage Form Name SUSPENSION
Route Name ORAL; RECTAL
Start Marketing Date 20110921
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 Sodium Polystyrene Sulfonate


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