Home > National Drug Code (NDC) > potassium chloride

potassium chloride - 68382-701-05 - (potassium chloride)

Alphabetical Index


Drug Information of potassium chloride

Product NDC: 68382-701
Proprietary Name: potassium chloride
Non Proprietary Name: potassium chloride
Active Ingredient(s): 750    mg/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: 68382-701
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018238
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20101025

Package Information of potassium chloride

Package NDC: 68382-701-05
Package Description: 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-701-05)

NDC Information of potassium chloride

NDC Code 68382-701-05
Proprietary Name potassium chloride
Package Description 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-701-05)
Product NDC 68382-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101025
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of potassium chloride


General Information