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Monopotassium phosphate

Generic Name
Monopotassium phosphate
Brand Names
Dextrose and Electrolyte No. 75, Ionosol-MB, Isolyte S, Isolyte S pH 7.4, Isoplate, K-phos, K-phos Neutral, K-phos No 2, Tis-U-sol
Drug Type
Small Molecule
Chemical Formula
H2KO4P
CAS Number
7778-77-0
Unique Ingredient Identifier
4J9FJ0HL51

Overview

Monopotassium phosphate, MKP, (also potassium dihydrogenphosphate, KDP, or monobasic potassium phosphate), KH2PO4, is a soluble salt of potassium and the dihydrogen phosphate ion. It is a source of phosphorus and potassium as well as a buffering agent. It can be used in fertilizer mixtures to reduce escape of ammonia by keeping pH low.

Indication

Used in buffers (determination of pH, pharmaceutical production, urinary acidifier, paper processing, baking powder, and food), nutrient solutions, yeast foods, special liquid fertilizers, sonar systems and other electronic applications; Used as a nutritional supplement in foods, a nonlinear optical material for laser use, and in wastewater treatment;

Associated Conditions

No associated conditions information available.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Baxter Healthcare Corporation
0338-0190
IRRIGATION
6.25 mg in 100 mL
2/21/2014
ICU Medical Inc.
0990-7372
INTRAVENOUS
15 mg in 100 mL
3/8/2021
Carilion Materials Management
68151-2193
ORAL
500 mg in 1 1
9/29/2014
Fresenius Kabi USA, LLC
65219-052
INTRAVENOUS
224 mg in 1 mL
11/30/2019
Amneal Pharmaceuticals Private Limited
80830-1692
INTRAVENOUS
224 mg in 1 mL
11/19/2023
American Regent, Inc.
0517-2051
INTRAVENOUS
224 mg in 1 mL
10/12/2023
Terumo BCT Ltd.
14537-408
INTRAVENOUS
0.00082 g in 100 mL
5/8/2015
American Regent, Inc.
0517-2505
INTRAVENOUS
224 mg in 1 mL
10/12/2023
Amneal Pharmaceuticals LLC
70121-1722
INTRAVENOUS
4.48 mg in 1 mL
7/22/2024
Fresenius Kabi USA, LLC
65219-056
INTRAVENOUS
224 mg in 1 mL
11/30/2019

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
DBL POTASSIUM DIHYDROGEN PHOSPHATE CONCENTRATED INJECTION
SIN05856P
INJECTION
1.361 g
5/21/1991

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
TIS-U-SOL SOLUTION
baxter corporation
00800007
Liquid - Irrigation
6.25 MG / 100 ML
12/31/1990
POTASSIUM PHOSPHATE INJ 3MMP/ML
hospira healthcare ulc
00351539
Solution - Intravenous
224 MG / ML
12/31/1980
NEUTRALITE LIQ
canadian custom packaging company
00313467
Liquid - Topical
34.3905 Kg / 576 L
12/31/1964
DEXTROSE 5% AND ELECTROLYTE NO75 INJ
baxter corporation
00261335
Liquid - Intravenous
100 MG / 100 ML
12/31/1990
POTASSIUM PHOSPHATES
00804789
Liquid - Intravenous
224 MG / ML
12/31/1989
POTASSIUM PHOSPHATE MONOBASIC INJECTION
00711306
Solution - Intravenous
176 MG / ML
12/31/1987
OMNIPLEX VIT AND MINERAL TAB
vita health products inc
00595810
Tablet - Oral
75 MG / TAB
12/31/1983
ISOLYTE S PH 7.4 (MULTI-ELECTROLYTE INJECTION)
b. braun medical inc
01931679
Solution - Intravenous
820 MCG / 100 ML
9/10/1996
POTASSIUM PHOSPHATES INJECTION, USP
fresenius kabi canada ltd
02139545
Solution - Intravenous
224 MG / ML
12/31/1984
ARTISIAL
jouveinal inc.
00642983
Liquid - Buccal
32.6 MG / 100 ML
12/31/1986

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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