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Lecithin, soybean

Generic Name
Lecithin, soybean
Drug Type
Small Molecule
CAS Number
8030-76-0
Unique Ingredient Identifier
1DI56QDM62

Overview

A complex mixture of phospholipids; glycolipids; and triglycerides; with substantial amounts of phosphatidylcholines; phosphatidylethanolamines; and phosphatidylinositols, which are sometimes loosely termed as 1,2-diacyl-3-phosphocholines. Lecithin is a component of the cell membrane and commercially extracted from soybeans and egg yolk. The emulsifying and surfactant properties are useful in food additives and for forming organogels (gels).

Indication

No indication information available.

Associated Conditions

  • Acne
  • Bulimia Nervosa
  • Obesity
  • Weight

Clinical Trials

Title
Posted
Study ID
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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
55154-4384
ORAL
N/A
7/24/2019
Mylan Pharmaceuticals Inc.
0378-3951
ORAL
N/A
12/9/2020
Mylan Pharmaceuticals Inc.
0378-3952
ORAL
N/A
12/9/2020
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
13411-856
ORAL
5 mg in 1 1
3/31/2025
Mylan Pharmaceuticals Inc.
0378-3953
ORAL
N/A
12/9/2020
Mylan Pharmaceuticals Inc.
0378-3950
ORAL
N/A
12/9/2020

EMA Drug Approvals

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No EMA approvals found for this drug.

HSA Drug Approvals

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Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

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Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

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No PPB approvals found for this drug.

TGA Drug Approvals

Health Canada Drug Approvals

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Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

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Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

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No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

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No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

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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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