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Potassium Chloride - 52125-098-02 - (POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride

Product NDC: 52125-098
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: 52125-098
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018279
Marketing Category: NDA
Start Marketing Date: 20120921

Package Information of Potassium Chloride

Package NDC: 52125-098-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-098-02)

NDC Information of Potassium Chloride

NDC Code 52125-098-02
Proprietary Name Potassium Chloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-098-02)
Product NDC 52125-098
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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


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