Klor-Con M - 0245-0150-01 - (Potassium Chloride)

Alphabetical Index


Drug Information of Klor-Con M

Product NDC: 0245-0150
Proprietary Name: Klor-Con M
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 1125    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 M

Product NDC: 0245-0150
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074726
Marketing Category: ANDA
Start Marketing Date: 20110118

Package Information of Klor-Con M

Package NDC: 0245-0150-01
Package Description: 10 BLISTER PACK in 1 CARTON (0245-0150-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-0150-89)

NDC Information of Klor-Con M

NDC Code 0245-0150-01
Proprietary Name Klor-Con M
Package Description 10 BLISTER PACK in 1 CARTON (0245-0150-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0245-0150-89)
Product NDC 0245-0150
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110118
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 1125
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Klor-Con M


General Information