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Potassium Chloride - 55154-3528-9 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 55154-3528
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 1500    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: 55154-3528
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074726
Marketing Category: ANDA
Start Marketing Date: 19981120

Package Information of Potassium Chloride

Package NDC: 55154-3528-9
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55154-3528-9)

NDC Information of Potassium Chloride

NDC Code 55154-3528-9
Proprietary Name Potassium Chloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55154-3528-9)
Product NDC 55154-3528
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 Cardinal Health
Substance Name POTASSIUM CHLORIDE
Strength Number 1500
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


General Information