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Potassium Chloride - 54868-4617-3 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 54868-4617
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 20    meq/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: 54868-4617
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075604
Marketing Category: ANDA
Start Marketing Date: 20020419

Package Information of Potassium Chloride

Package NDC: 54868-4617-3
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4617-3)

NDC Information of Potassium Chloride

NDC Code 54868-4617-3
Proprietary Name Potassium Chloride
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4617-3)
Product NDC 54868-4617
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020419
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 20
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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