Potassium Citrate

FDA Approved: * October 13, 1988
Pharm Company: * MISSION PHARMA
Category: Urinary System

Potassium citrate (also known as tripotassium citrate) is a potassium salt of citric acid with the molecular formula K3C6H5O7. It is a white, hygroscopic crystalline powder. It is odorless with a saline taste. It contains 38.28% potassium by mass. In the monohydrate form, it is highly hygroscopic and deliquescent. As a food additive, potassium citrate is used to regulate acidity, and is known as E number E332. Medicinally, it may be used to control kidney stones derived from uric acid or cyst... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
19 Discussions

Dosage List

Potassium Citrate USL;070
Potassium Citrate 540 mg Extended Release Tablet
NDC: 0245-0070
Labeler:
Upsher-smith Laboratories, Inc.
Potassium Citrate USL;071
Potassium Citrate 1080 mg Extended Release Tablet
NDC: 0245-0071
Labeler:
Upsher-smith Laboratories, Inc.
Potassium Citrate M15
Potassium Citrate 15 Meq/1 Oral Tablet
NDC: 44523-415
Labeler:
Biocomp Pharma, Inc.
Potassium Citrate 5 Meq/1 Oral Tablet, Extended Release
NDC: 0591-2682
Labeler:
Actavis Pharma, Inc.
Potassium Citrate 10 Meq/1 Oral Tablet, Extended Release
NDC: 0591-2729
Labeler:
Actavis Pharma, Inc.
Potassium Citrate 15 Meq/1 Oral Tablet, Extended Release
NDC: 0591-2742
Labeler:
Actavis Pharma, Inc.
Potassium Citrate 5 Meq/1 Oral Tablet, Extended Release
NDC: 31722-129
Labeler:
Camber Pharmaceuticals, Inc
Potassium Citrate 10 Meq/1 Oral Tablet, Extended Release
NDC: 31722-130
Labeler:
Camber Pharmaceuticals, Inc
Potassium Citrate 15 Meq/1 Oral Tablet, Extended Release
NDC: 31722-132
Labeler:
Camber Pharmaceuticals, Inc
Kali Citricum 6 [Hp_c]/1 Oral Pellet
NDC: 37662-2461
Labeler:
Hahnemann Laboratories, Inc.
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