Potassium
Potassium Chloride
The FDA lists this product in 60 strengths and forms.
Composition
- Active ingredients
- POTASSIUM CHLORIDE 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- POTASSIUM CHLORIDE 2MEQ/ML · InjectableANDA086713-001 · Discontinued
- POTASSIUM CHLORIDE 2MEQ/ML · InjectableANDA087362-001 · Discontinued
- POTASSIUM CHLORIDE 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended releaseThis page
- POTASSIUM CHLORIDE 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Tablet, extended releaseNDA019439-002 · Discontinued
- POTASSIUM CHLORIDE 8MEQ · Tablet, extended releaseANDA206759-001 · Prescription
- POTASSIUM CHLORIDE 10MEQ · Tablet, extended releaseANDA206759-002 · Prescription
- POTASSIUM CHLORIDE 20MEQ · For solutionANDA211667-001 · Prescription
- POTASSIUM CHLORIDE 20MEQ · For solutionANDA213467-001 · Prescription
- POTASSIUM CHLORIDE 20MEQ · Tablet, extended releaseANDA216269-003 · Prescription
- POTASSIUM CHLORIDE 10MEQ · Tablet, extended release
At a glance
- Brand name
- Potassium Chloride
- Drug class
- Potassium, Electrolyte solutions
- Route
- Oral
- Dosage form
- Tablet, extended release
- Applicant
- Schering
- Status
- Discontinued
- FDA approval
- 13 Jun 1986
- Application
- NDA019439-001
- RxCUI
- 8591