Klor-Con - 0245-0035-30 - (Potassium Chloride)

Alphabetical Index


Drug Information of Klor-Con

Product NDC: 0245-0035
Proprietary Name: Klor-Con
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 20    meq/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Klor-Con

Product NDC: 0245-0035
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091101

Package Information of Klor-Con

Package NDC: 0245-0035-30
Package Description: 30 PACKET in 1 CARTON (0245-0035-30) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0035-89)

NDC Information of Klor-Con

NDC Code 0245-0035-30
Proprietary Name Klor-Con
Package Description 30 PACKET in 1 CARTON (0245-0035-30) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0035-89)
Product NDC 0245-0035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name POWDER, FOR SOLUTION
Route Name ORAL
Start Marketing Date 20091101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 20
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Klor-Con


General Information