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Potassium Chloride - 54868-1317-5 - (potassium chloride)

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Drug Information of Potassium Chloride

Product NDC: 54868-1317
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: 54868-1317
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070980
Marketing Category: ANDA
Start Marketing Date: 19960411

Package Information of Potassium Chloride

Package NDC: 54868-1317-5
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-1317-5)

NDC Information of Potassium Chloride

NDC Code 54868-1317-5
Proprietary Name Potassium Chloride
Package Description 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-1317-5)
Product NDC 54868-1317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19960411
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


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