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Drug ReportsLecithin
Lecithin
Imagent (lecithin) is a small molecule pharmaceutical. Lecithin was first approved as Imagent on 2002-05-31. It is used to treat mental fatigue in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
signs and symptoms pathological conditionsD013568
behavior and behavior mechanismsD001520
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
Brand Name
Status
Last Update
debaochununapproved drug other2022-02-22
jba joint reviveunapproved drug other2025-03-31
the melanin skin protectant creamunapproved drug other2025-05-01
Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
V08: Contrast media
V08C: Magnetic resonance imaging contrast media
V08CX: Other magnetic resonance imaging contrast media in atc
V08CX01: Perflubron
HCPCS
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Clinical
Clinical Trials
173 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients11
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLecithin
INNperflubron
Description
Lecithin (/ˈlɛsɪθɪn/ LESS-ith-in; from the Ancient Greek λέκιθος lékithos "yolk") is a generic term to designate any group of yellow-brownish fatty substances occurring in animal and plant tissues which are amphiphilic – they attract both water and fatty substances (and so are both hydrophilic and lipophilic), and are used for smoothing food textures, emulsifying, homogenizing liquid mixtures, and repelling sticking materials.
Classification
Small molecule
Drug class
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Structure (InChI/SMILES or Protein Sequence)
C[N+](C)(C)CCOP(=O)([O-])OCC(COC=O)OC=O
Identifiers
PDB
CAS-ID93685-90-6
RxCUI
ChEMBL IDCHEMBL2107798
ChEBI ID
PubChem CID
DrugBank
UNII IDQ1D0Q7R4D9 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
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Safety
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322 adverse events reported
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