MedPath

Potassium sulfate

Generic Name
Potassium sulfate
Brand Names
Suprep Bowel Prep Kit
Drug Type
Small Molecule
Chemical Formula
K2O4S
CAS Number
7778-80-5
Unique Ingredient Identifier
1K573LC5TV

Overview

No overview information available.

Background

No background information available.

Indication

Potassium is used to regulate hypokalemia as a primary condition or secondary to other medical conditions.

Associated Conditions

No associated conditions information available.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Ascend Laboratories, LLC
67877-725
ORAL
3.13 g in 177 mL
3/28/2023
Bestmade Natural Products
82969-9015
ORAL
6 [hp_X] in 6 [hp_X]
3/23/2025
Strides Pharma Science Limited
64380-116
ORAL
3.13 g in 177 mL
1/17/2024
Taro Pharmaceuticals U.S.A., inc.
51672-4170
ORAL
3.13 g in 177 mL
4/2/2024
Braintree Laboratories, Inc.
52268-112
ORAL
2.35 g in 133.1 mL
8/18/2020
Bestmade Natural Products
82969-3019
ORAL
6 [hp_X] in 6 [hp_X]
1/22/2025
Bestmade Natural Products
82969-3020
ORAL
6 [hp_X] in 6 [hp_X]
1/22/2025
Lupin Pharmaceuticals, Inc.
43386-700
ORAL
3.13 g in 177 mL
12/20/2023
Novel Laboratories, Inc.
40032-700
ORAL
3.13 g in 177 mL
12/4/2017
Bestmade Natural Products
82969-3011
ORAL
6 [hp_X] in 6 [hp_X]
1/22/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

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