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Potassium Chloride - 62037-999-05 - (potassium chloride)

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Drug Information of Potassium Chloride

Product NDC: 62037-999
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: 62037-999
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076368
Marketing Category: ANDA
Start Marketing Date: 20040818

Package Information of Potassium Chloride

Package NDC: 62037-999-05
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-999-05)

NDC Information of Potassium Chloride

NDC Code 62037-999-05
Proprietary Name Potassium Chloride
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-999-05)
Product NDC 62037-999
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040818
Marketing Category Name ANDA
Labeler Name Watson Pharma, 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


General Information