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Potassium Chloride - 0781-1516-01 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 0781-1516
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 600    mg/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 0781-1516
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 19860417

Package Information of Potassium Chloride

Package NDC: 0781-1516-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-1516-01)

NDC Information of Potassium Chloride

NDC Code 0781-1516-01
Proprietary Name Potassium Chloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-1516-01)
Product NDC 0781-1516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19860417
Marketing Category Name NDA
Labeler Name Sandoz Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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