Kalexate - 10702-036-45 - (Sodium Polystyrene Sulfonate)

Alphabetical Index


Drug Information of Kalexate

Product NDC: 10702-036
Proprietary Name: Kalexate
Non Proprietary Name: Sodium Polystyrene Sulfonate
Active Ingredient(s): 1    mg/g & nbsp;   Sodium Polystyrene Sulfonate
Administration Route(s): ORAL; RECTAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of Kalexate

Product NDC: 10702-036
Labeler Name: KVK-Tech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040905
Marketing Category: ANDA
Start Marketing Date: 20120725

Package Information of Kalexate

Package NDC: 10702-036-45
Package Description: 454 g in 1 JAR (10702-036-45)

NDC Information of Kalexate

NDC Code 10702-036-45
Proprietary Name Kalexate
Package Description 454 g in 1 JAR (10702-036-45)
Product NDC 10702-036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Polystyrene Sulfonate
Dosage Form Name POWDER
Route Name ORAL; RECTAL
Start Marketing Date 20120725
Marketing Category Name ANDA
Labeler Name KVK-Tech, Inc.
Substance Name SODIUM POLYSTYRENE SULFONATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Kalexate


General Information