Klor-Con - 0245-0041-00 - (Potassium Chloride)

Alphabetical Index


Drug Information of Klor-Con

Product NDC: 0245-0041
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: 0245-0041
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 19860417

Package Information of Klor-Con

Package NDC: 0245-0041-00
Package Description: 1 BAG in 1 BOX (0245-0041-00) > 10000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG

NDC Information of Klor-Con

NDC Code 0245-0041-00
Proprietary Name Klor-Con
Package Description 1 BAG in 1 BOX (0245-0041-00) > 10000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG
Product NDC 0245-0041
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 Upsher-Smith Laboratories, 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