Klor Con M - 0615-3599-30 - (potassium chloride)

Alphabetical Index


Drug Information of Klor Con M

Product NDC: 0615-3599
Proprietary Name: Klor Con M
Non Proprietary Name: potassium chloride
Active Ingredient(s): 20    meq/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: 0615-3599
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074726
Marketing Category: ANDA
Start Marketing Date: 19981120

Package Information of Klor Con M

Package NDC: 0615-3599-30
Package Description: 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-3599-30) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Klor Con M

NDC Code 0615-3599-30
Proprietary Name Klor Con M
Package Description 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-3599-30) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 0615-3599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981120
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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 M


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