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Potassium Chloride - 0574-0181-05 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 0574-0181
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: 0574-0181
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200185
Marketing Category: ANDA
Start Marketing Date: 20110603

Package Information of Potassium Chloride

Package NDC: 0574-0181-05
Package Description: 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0574-0181-05)

NDC Information of Potassium Chloride

NDC Code 0574-0181-05
Proprietary Name Potassium Chloride
Package Description 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0574-0181-05)
Product NDC 0574-0181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110603
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, 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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