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Potassium Citrate - 0245-0071-11 - (potassium citrate)

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Drug Information of Potassium Citrate

Product NDC: 0245-0071
Proprietary Name: Potassium Citrate
Non Proprietary Name: potassium citrate
Active Ingredient(s): 10    meq/1 & nbsp;   potassium citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Citrate

Product NDC: 0245-0071
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019071
Marketing Category: NDA
Start Marketing Date: 20060901

Package Information of Potassium Citrate

Package NDC: 0245-0071-11
Package Description: 100 TABLET in 1 BOTTLE (0245-0071-11)

NDC Information of Potassium Citrate

NDC Code 0245-0071-11
Proprietary Name Potassium Citrate
Package Description 100 TABLET in 1 BOTTLE (0245-0071-11)
Product NDC 0245-0071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060901
Marketing Category Name NDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name POTASSIUM CITRATE
Strength Number 10
Strength Unit meq/1
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of Potassium Citrate


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