Home > National Drug Code (NDC) > Potassium Chloride

Potassium Chloride - 62037-559-10 - (Potassium Chloride)

Alphabetical Index


Drug Information of Potassium Chloride

Product NDC: 62037-559
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 8    meq/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 62037-559
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077419
Marketing Category: ANDA
Start Marketing Date: 20080825

Package Information of Potassium Chloride

Package NDC: 62037-559-10
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-559-10)

NDC Information of Potassium Chloride

NDC Code 62037-559-10
Proprietary Name Potassium Chloride
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-559-10)
Product NDC 62037-559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080825
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 8
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


General Information