Klor-Con - 24236-875-20 - (Potassium Chloride)

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Drug Information of Klor-Con

Product NDC: 24236-875
Proprietary Name: Klor-Con
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 750    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: 24236-875
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 20130318

Package Information of Klor-Con

Package NDC: 24236-875-20
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CANISTER (24236-875-20)

NDC Information of Klor-Con

NDC Code 24236-875-20
Proprietary Name Klor-Con
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CANISTER (24236-875-20)
Product NDC 24236-875
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 20130318
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Klor-Con


General Information