MedPath

Tyrosine

Generic Name
Tyrosine
Brand Names
Premasol, Clinimix E 2.75/5, Aminosyn-PF 7%, Primene, Clinimix 2.75/5, Trophamine 10 %, Plenamine, Olimel, Prosol, Clinisol 15, Periolimel, Travasol 10
Drug Type
Small Molecule
Chemical Formula
C9H11NO3
CAS Number
60-18-4
Unique Ingredient Identifier
42HK56048U

Overview

Tyrosine is a non-essential amino acid. In animals it is synthesized from phenylalanine. It is also the precursor of epinephrine, thyroid hormones, and melanin.

Indication

Tyrosine is claimed to act as an effective antidepressant, however results are mixed. Tyrosine has also been claimed to reduce stress and combat narcolepsy and chronic fatigue, however these claims have been refuted by some studies.

Associated Conditions

  • Acute Renal Dysfunction
  • Renal Failure, Chronic Renal Failure

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/10/08
N/A
Active, not recruiting
First Hospital of China Medical University
2023/04/21
N/A
Recruiting
2022/08/11
Phase 1
Terminated
2022/05/19
N/A
Completed
2022/02/11
Phase 3
Recruiting
2021/02/18
Phase 2
Not yet recruiting
Second Affiliated Hospital, School of Medicine, Zhejiang University
2020/09/16
Not Applicable
Completed
Direction Centrale du Service de Santé des Armées
2020/08/19
Not Applicable
Completed
Direction Centrale du Service de Santé des Armées
2020/06/19
Phase 2
Not yet recruiting
wang, jianxiang
2020/05/05
N/A
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Baxter Healthcare Corporation
0338-0184
INTRAVENOUS
32 mg in 100 mL
4/13/2021
Baxter Healthcare Company
0338-0210
INTRAVENOUS
32 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-0210
INTRAVENOUS
32 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-1089
INTRAVENOUS
17 mg in 100 mL
4/13/2021
Baxter Healthcare Corporation
0338-1099
INTRAVENOUS
20 mg in 100 mL
4/13/2021
Baxter Healthcare Corporation
0338-0194
INTRAVENOUS
32 mg in 100 mL
4/13/2021
Baxter Healthcare Company
0338-1147
INTRAVENOUS
20 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-1147
INTRAVENOUS
20 mg in 100 mL
9/21/2020
Baxter Healthcare Company
0338-1142
INTRAVENOUS
11 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-1142
INTRAVENOUS
11 mg in 100 mL
9/21/2020

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA 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

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
4.25% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 10% DEXTROSE
baxter corporation clintec nutrition division
N/A
Solution - Intravenous
17 MG / 100 ML
12/31/1996
4.25% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTRLYTES IN 10% DEXTROSE
baxter corporation clintec nutrition division
N/A
Solution - Intravenous
17 MG / 100 ML
12/31/1996
2.75%TRAVASOL AMINO ACID INJ.W.ELEC.W.5%DEX.
clintec nutrition company
02143240
Liquid - Intravenous
11 MG / 100 ML
12/31/1996
4.25%TRAVASOL AMINO ACID INJ.W.ELECW.5%DEX.
clintec nutrition company
02143224
Liquid - Intravenous
17 MG / 100 ML
12/31/1996
5% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTROLYTES IN 25% DEXTROSE
baxter corporation clintec nutrition division
02142244
Solution - Intravenous
20 MG / 100 ML
12/31/1996
2.5% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 10% DEXTROSE CLINIMIX
baxter corporation clintec nutrition division
02013975
Solution - Intravenous
10 MG / 100 ML
12/31/1993
CLINIMIX E
baxter corporation
02013967
Solution - Intravenous
20 MG / 100 ML
12/31/1993
5% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTROLYTES IN 20% DEXTROSE
baxter corporation clintec nutrition division
02142252
Solution - Intravenous
20 MG / 100 ML
12/31/1996
5% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 20% DEXTROSE
baxter corporation clintec nutrition division
02142368
Solution - Intravenous
20 MG / 100 ML
12/31/1996
4.25% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTROLYTES IN 25% DEXTROSE
baxter corporation clintec nutrition division
02142295
Solution - Intravenous
17 MG / 100 ML
12/31/1996

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
NEPHROTECT SOLUCION PARA PERFUSION
67038
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
PEDIAVEN G20 SOLUCION PARA PERFUSION
Fresenius Kabi España, S.A.U.
78951
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Not Commercialized
SMOFKABIVEN PERIFERICO EMULSION PARA PERFUSION
Fresenius Kabi España, S.A.U.
70513
EMULSIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
SMOFKABIVEN EXTRA NITROGEN EMULSION PARA PERFUSION
Fresenius Kabi España, S.A.U.
82509
EMULSIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
SMOFKABIVEN SIN ELECTROLITOS CENTRAL EMULSION PARA PERFUSION
Fresenius Kabi España, S.A.U.
70892
EMULSIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
SYNTHAMIN 17 REFORMULADO SOLUCION PARA PERFUSION
Baxter S.L.
58196
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
NUMETA G19%E, EMULSION PARA PERFUSION
Baxter S.L.
74020
EMULSIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
SYNTHAMIN 17 REFORMULADO SIN ELECTROLITOS SOLUCION PARA PERFUSION
Baxter S.L.
58197
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
ISOPLASMAL G SOLUCION PARA PERFUSION
B Braun Medical S.A.
59737
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Commercialized
TAURAMIN 8% , SOLUCION PARA PERFUSION
Laboratorios Grifols S.A.
65936
SOLUCIÓN PARA PERFUSIÓN
Uso Hospitalario
Not Commercialized

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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.