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potassium chloride - 68084-419-01 - (potassium chloride)

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Drug Information of potassium chloride

Product NDC: 68084-419
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: 68084-419
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018238
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120702

Package Information of potassium chloride

Package NDC: 68084-419-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-419-01) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-419-11)

NDC Information of potassium chloride

NDC Code 68084-419-01
Proprietary Name potassium chloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-419-01) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-419-11)
Product NDC 68084-419
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120702
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name American Health Packaging
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