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Potassium Chloride - 0781-5720-10 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 0781-5720
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 750    mg/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 0781-5720
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074726
Marketing Category: ANDA
Start Marketing Date: 19981120

Package Information of Potassium Chloride

Package NDC: 0781-5720-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5720-10)

NDC Information of Potassium Chloride

NDC Code 0781-5720-10
Proprietary Name Potassium Chloride
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5720-10)
Product NDC 0781-5720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981120
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


General Information