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Potassium Citrate - 54868-5644-0 - (potassium citrate)

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Drug Information of Potassium Citrate

Product NDC: 54868-5644
Proprietary Name: Potassium Citrate
Non Proprietary Name: potassium citrate
Active Ingredient(s): 1080    mg/1 & nbsp;   potassium citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Citrate

Product NDC: 54868-5644
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077440
Marketing Category: ANDA
Start Marketing Date: 20060724

Package Information of Potassium Citrate

Package NDC: 54868-5644-0
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5644-0)

NDC Information of Potassium Citrate

NDC Code 54868-5644-0
Proprietary Name Potassium Citrate
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5644-0)
Product NDC 54868-5644
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium citrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060724
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name POTASSIUM CITRATE
Strength Number 1080
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Citrate


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