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Medicines · US (FDA)

FDA 2024

FDA

Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate

Approved 15 Jul 2024OralSolution

The FDA lists this product in 7 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionThis page
MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA215469-001 · Prescription
MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA206431-001 · Prescription
MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA202511-001 · Prescription
MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA212903-001 · Prescription
MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA204135-001 · Prescription

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

MAGNESIUM SULFATE 1.6GM/BOT; POTASSIUM SULFATE 3.13GM/BOT; SODIUM SULFATE 17.5GM/BOT · SolutionANDA213924-001 · Prescription

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA209941.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Brand name: Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate
Active substance: magnesium sulfate
Route: Oral
Dosage form: Solution
Applicant: Pai Holdings
Status: Prescription
FDA approval: 15 Jul 2024
Application: ANDA209941-001