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Potassium Chloride - 42291-679-90 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 42291-679
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): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 42291-679
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077419
Marketing Category: ANDA
Start Marketing Date: 20130305

Package Information of Potassium Chloride

Package NDC: 42291-679-90
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-679-90)

NDC Information of Potassium Chloride

NDC Code 42291-679-90
Proprietary Name Potassium Chloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-679-90)
Product NDC 42291-679
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130305
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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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