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Potassium Chloride - 0085-1718-02 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 0085-1718
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: 0085-1718
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019439
Marketing Category: NDA
Start Marketing Date: 19860613

Package Information of Potassium Chloride

Package NDC: 0085-1718-02
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-1718-02)

NDC Information of Potassium Chloride

NDC Code 0085-1718-02
Proprietary Name Potassium Chloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-1718-02)
Product NDC 0085-1718
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19860613
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
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


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