Klor-Con - 53808-0375-1 - (Potassium Chloride)

Alphabetical Index


Drug Information of Klor-Con

Product NDC: 53808-0375
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Klor-Con

Product NDC: 53808-0375
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 20090701

Package Information of Klor-Con

Package NDC: 53808-0375-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0375-1)

NDC Information of Klor-Con

NDC Code 53808-0375-1
Proprietary Name Klor-Con
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0375-1)
Product NDC 53808-0375
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name NDA
Labeler Name State of Florida DOH Central Pharmacy
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