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Potassium Chloride - 63739-446-04 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 63739-446
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 10    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: 63739-446
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074726
Marketing Category: ANDA
Start Marketing Date: 20090803

Package Information of Potassium Chloride

Package NDC: 63739-446-04
Package Description: 10 BLISTER PACK in 1 BOX (63739-446-04) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Potassium Chloride

NDC Code 63739-446-04
Proprietary Name Potassium Chloride
Package Description 10 BLISTER PACK in 1 BOX (63739-446-04) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 63739-446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090803
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name POTASSIUM CHLORIDE
Strength Number 10
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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