Klor-Con - 67544-154-53 - (Potassium Chloride)

Alphabetical Index


Drug Information of Klor-Con

Product NDC: 67544-154
Proprietary Name: Klor-Con
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 600    mg/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Klor-Con

Product NDC: 67544-154
Labeler Name: Aphena Pharma Solutions - Tennessee, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 19860417

Package Information of Klor-Con

Package NDC: 67544-154-53
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-154-53)

NDC Information of Klor-Con

NDC Code 67544-154-53
Proprietary Name Klor-Con
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (67544-154-53)
Product NDC 67544-154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19860417
Marketing Category Name NDA
Labeler Name Aphena Pharma Solutions - Tennessee, LLC
Substance Name POTASSIUM CHLORIDE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Klor-Con


General Information