MedPath

Proline

Generic Name
Proline
Brand Names
Aminosyn II 7 %, Sulfite-free, Aminosyn-PF 7%, Clinimix 2.75/5, Clinimix E 2.75/5, Clinisol 15, Freamine 6.9, Freamine III 10, Hepatamine 8, Olimel, Periolimel, Plenamine, Premasol, Primene, Procalamine 3, Prosol, Travasol 10, Trophamine 10 %
Drug Type
Small Molecule
Chemical Formula
C5H9NO2
CAS Number
147-85-3
Unique Ingredient Identifier
9DLQ4CIU6V

Overview

Proline is one of the twenty amino acids used in living organisms as the building blocks of proteins. Proline is sometimes called an imino acid, although the IUPAC definition of an imine requires a carbon-nitrogen double bond. Proline is a non-essential amino acid that is synthesized from glutamic acid. It is an essential component of collagen and is important for proper functioning of joints and tendons.

Indication

L-Proline is extremely important for the proper functioning of joints and tendons and also helps maintain and strengthen heart muscles.

Associated Conditions

No associated conditions information available.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Baxter Healthcare Corporation
0338-0184
INTRAVENOUS
544 mg in 100 mL
4/13/2021
Baxter Healthcare Company
0338-0210
INTRAVENOUS
544 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-0210
INTRAVENOUS
544 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-1089
INTRAVENOUS
289 mg in 100 mL
4/13/2021
Baxter Healthcare Corporation
0338-1099
INTRAVENOUS
340 mg in 100 mL
4/13/2021
ICU Medical Inc.
0990-7171
INTRAVENOUS
1083 mg in 100 mL
5/4/2022
Baxter Healthcare Corporation
0338-0194
INTRAVENOUS
544 mg in 100 mL
4/13/2021
Baxter Healthcare Company
0338-1147
INTRAVENOUS
340 mg in 100 mL
9/21/2020
Baxter Healthcare Corporation
0338-1147
INTRAVENOUS
340 mg in 100 mL
9/21/2020
Baxter Healthcare Company
0338-1142
INTRAVENOUS
187 mg in 100 mL
9/21/2020

EMA Drug Approvals

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

HSA Drug Approvals

NMPA Drug Approvals

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

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
289 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
289 MG / 100 ML
12/31/1996
2.75%TRAVASOL AMINO ACID INJ.W.ELEC.W.5%DEX.
clintec nutrition company
02143240
Liquid - Intravenous
187 MG / 100 ML
12/31/1996
4.25%TRAVASOL AMINO ACID INJ.W.ELECW.5%DEX.
clintec nutrition company
02143224
Liquid - Intravenous
289 MG / 100 ML
12/31/1996
5% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTROLYTES IN 25% DEXTROSE
baxter corporation clintec nutrition division
02142244
Solution - Intravenous
340 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
105 MG / 100 ML
12/31/1993
CLINIMIX E
baxter corporation
02013967
Solution - Intravenous
210 MG / 100 ML
12/31/1993
5% TRAVASOL AMINO ACID INJECTION WITHOUT ELECTROLYTES IN 20% DEXTROSE
baxter corporation clintec nutrition division
02142252
Solution - Intravenous
340 MG / 100 ML
12/31/1996
5% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 20% DEXTROSE
baxter corporation clintec nutrition division
02142368
Solution - Intravenous
340 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
289 MG / 100 ML
12/31/1996

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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