Friday, July 10, 2026

Drug profile · INN

potassium citrate

potassium citrate (NULL) is an FDA-listed pharmaceutical active ingredient. Associated with Teva Pharma GmbH. Route of administration: oral. Current US regulatory status: approved.

FDA: approved EMA: approved TGA: approved Alimentary tract and metabolism (A12) A12BA30
US status approved
Patents linked 1
Pipeline programs 1
News articles 1
Drug details — potassium citrate
US status
approved
Class
Alimentary tract and metabolism (A12)
Route
ORAL
Patents
1
Programs
1
Data quality
0.89

Quick answer

potassium citrate (NULL) is an FDA-listed pharmaceutical active ingredient. Associated with Teva Pharma GmbH. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN potassium citrate
Brand NULL
Therapeutic class Alimentary tract and metabolism (A12)
Route ORAL
Formulation FOR SOLUTION
ATC code A12BA30

Approval history

Authority Status Date
FDA approved
EMA approved
TGA approved

Recent coverage

Pipeline programs

  1. potassium citrate Phase 3 · Ultragenyx UK · Hypercalciuria

Related & competitor drugs

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  4. aprepitant Alimentary tract and metabolism (A04)
  5. budesonide Alimentary tract and metabolism (A07)
  6. canagliflozin Alimentary tract and metabolism (A10)
  1. US 9295659

    High dose extended-release potassium citrate wax matrix tablet

    Expires Mon Mar 24 2036 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is potassium citrate?

potassium citrate (NULL) is an FDA-listed pharmaceutical active ingredient. Associated with Teva Pharma GmbH. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for potassium citrate?

NULL is a marketed brand name for potassium citrate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of potassium citrate?

potassium citrate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.