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Sodium phosphate, monobasic, unspecified form

Generic Name
Sodium phosphate, monobasic, unspecified form
Brand Names
Fleet Mineral Oil, Pedia-lax Liquid, Urogesic Blue Reformulated Apr 2012, Utira
Drug Type
Small Molecule
Unique Ingredient Identifier
3980JIH2SW

Overview

No overview information available.

Indication

Used to treat constipation or to clean the bowel before a colonoscopy .

Associated Conditions

  • Constipation
  • Occasional Constipation

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Cardinal Health 107, LLC
55154-5777
ORAL
500 mg in 5 mL
6/21/2019
Fenwal, Inc.
0942-0641
INTRAVENOUS
11 g in 500 mL
2/11/2022
Terumo BCT Vietnam CO., Ltd.
82906-506
INTRAVENOUS
0.176 g in 70 mL
3/1/2023
Arteriocyte Medical Systems, Inc.
43203-852
EXTRACORPOREAL
0.220 g in 10 mL
12/17/2018
Terumo BCT Ltd
14537-967
INTRAVENOUS
2.2 g in 100 mL
1/10/2019
Baxter Healthcare Corporation
24571-123
EXTRACORPOREAL
5.29 g in 1000 mL
8/13/2020
Fenwal, Inc.
0942-9005
INTRAVENOUS
2.2 g in 100 mL
11/1/2022
Terumo BCT Ltd
14537-966
INTRAVENOUS
0.588 g in 100 mL
12/4/2018
Dr. Donna Restivo DC
62185-0065
ORAL
30 [hp_X] in 1 mL
5/23/2025
Terumo Corporation
53877-010
INTRAVENOUS
156 mg in 70 mL
12/10/2021

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

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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