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Moxaverine
Moxaverine is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
A: Alimentary tract and metabolism drugs
A03: Drugs for functional gastrointestinal disorders
A03A: Drugs for functional gastrointestinal disorders
A03AD: Papaverine and derivatives containing drugs for functional gastrointestinal disorders
A03AD30: Moxaverine
HCPCS
No data
Clinical
Clinical Trials
4 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Regional blood flowD012039212
Macular degenerationD008268EFO_0001365H35.30111
GlaucomaD005901EFO_0000516H40111
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Ocular physiological phenomenaD00979911
IschemiaD007511EFO_000055611
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMOXAVERINE
INNmoxaverine
Description
Moxaverine is a member of isoquinolines.
Classification
Small molecule
Drug classspasmolytic agents (papaverine type)
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CCc1cc2cc(OC)c(OC)cc2c(Cc2ccccc2)n1
Identifiers
PDB
CAS-ID10539-19-2
RxCUI52918
ChEMBL IDCHEMBL2105060
ChEBI ID
PubChem CID70882
DrugBankDB12251
UNII IDP3P08Y1XJ4 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
Mock data
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Additional graphs summarizing 27 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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