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Drug ReportsMebendazole
Mebendazole
Emverm (mebendazole) is a small molecule pharmaceutical. Mebendazole was first approved as Vermox on 1982-01-01. It is used to treat ancylostomiasis, ascariasis, enterobiasis, helminthiasis, and trichuriasis in the USA.
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Financial
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Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
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FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
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Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
Trade Name
FDA
EMA
Emverm (discontinued: Vermox)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Mebendazole
Tradename
Company
Number
Date
Products
VERMOXJohnson & JohnsonN-017481 DISCN1982-01-01
1 products, RLD
VERMOXJohnson & JohnsonN-208398 DISCN2016-10-19
1 products, RLD
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Labels
FDA
EMA
Brand Name
Status
Last Update
emvermANDA2021-08-23
mebendazoleANDA2010-04-29
vermoxNew Drug Application2021-10-05
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
P: Antiparasitic products, insecticides and repellents
P02: Anthelmintics
P02C: Antinematodal agents
P02CA: Benzimidazole derivatives, antinematodal
P02CA01: Mebendazole
P02CA51: Mebendazole, combinations
HCPCS
No data
Clinical
Clinical Trials
49 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_0000544224210
Communicable diseasesD00314112317
Hookworm infectionsD006725EFO_0007314B762237
AncylostomiasisD000724EFO_0007145B76.02226
HelminthiasisD006373EFO_1001342B65-B832125
TrichuriasisD014257EFO_0007524B791225
Parasitic diseasesD010272EFO_0001067B88134
MalnutritionD044342EFO_0008572E40-E461113
Drug resistanceD004351Z16.3011
AncylostomatoideaD00072311
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C803215
AnemiaD000740EFO_0004272D64.9224
Healthy volunteers/patients213
Colorectal neoplasmsD015179112
EnterobiasisD017229B8022
VomitingD014839R11.111
NecatoriasisD009332EFO_0007390B76.111
Birth weightD001724EFO_000434411
Infant mortalityD00722611
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
GlioblastomaD005909EFO_0000515313
GliomaD005910EFO_0000520313
AstrocytomaD001254EFO_0000271212
Brain stem neoplasmsD020295EFO_1001767212
Cocaine-related disordersD019970F14112
CarcinomaD002277C80.01112
Breast neoplasmsD001943EFO_0003869C5011
Lung neoplasmsD008175C34.9011
SarcomaD01250911
Central nervous system neoplasmsD01654311
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Brain neoplasmsD001932EFO_0003833C7122
MedulloblastomaD00852711
OligodendrogliomaD009837EFO_000063111
Indications Without Phase
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMebendazole
INNmebendazole
Description
Mebendazole is a carbamate ester that is methyl 1H-benzimidazol-2-ylcarbamate substituted by a benzoyl group at position 5. It has a role as an antinematodal drug, a tubulin modulator and a microtubule-destabilising agent. It is a member of benzimidazoles, a carbamate ester and an aromatic ketone. It derives from a hydride of a 1H-benzimidazole.
Classification
Small molecule
Drug classantithelmintics (tibendazole type)
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
COC(=O)Nc1nc2cc(C(=O)c3ccccc3)ccc2[nH]1
Identifiers
PDB
CAS-ID31431-39-7
RxCUI
ChEMBL IDCHEMBL685
ChEBI ID6704
PubChem CID4030
DrugBankDB00643
UNII ID81G6I5V05I (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
No data
Estimated US medical usage
Mebendazole
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Number of purchases
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Refill frequency
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Price per prescription (USD)
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 7,063 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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768 adverse events reported
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