Home > National Drug Code (NDC) > Potassium Chloride

Potassium Chloride - 0245-0243-11 - (Potassium Chloride)

Alphabetical Index


Drug Information of Potassium Chloride

Product NDC: 0245-0243
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 750    mg/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: 0245-0243
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 Potassium Chloride

Package NDC: 0245-0243-11
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0245-0243-11)

NDC Information of Potassium Chloride

NDC Code 0245-0243-11
Proprietary Name Potassium Chloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0245-0243-11)
Product NDC 0245-0243
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, 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 Potassium Chloride


General Information