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Potassium Chloride - 0615-1318-39 - (Potassium)

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Drug Information of Potassium Chloride

Product NDC: 0615-1318
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium
Active Ingredient(s): 750    mg/1 & nbsp;   Potassium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 0615-1318
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077419
Marketing Category: ANDA
Start Marketing Date: 20080602

Package Information of Potassium Chloride

Package NDC: 0615-1318-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-1318-39)

NDC Information of Potassium Chloride

NDC Code 0615-1318-39
Proprietary Name Potassium Chloride
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-1318-39)
Product NDC 0615-1318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080602
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Potassium Chloride


General Information