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Potassium Chloride - 55154-3328-0 - (potassium chloride)

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Drug Information of Potassium Chloride

Product NDC: 55154-3328
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): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 55154-3328
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075604
Marketing Category: ANDA
Start Marketing Date: 20090825

Package Information of Potassium Chloride

Package NDC: 55154-3328-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3328-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Potassium Chloride

NDC Code 55154-3328-0
Proprietary Name Potassium Chloride
Package Description 10 BLISTER PACK in 1 BAG (55154-3328-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-3328
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090825
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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