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Drug ReportsTrimethobenzamide
Trimethobenzamide
Tigan, Trimethobenzamide (trimethobenzamide) is a small molecule pharmaceutical. Trimethobenzamide was first approved as Tigan on 1982-01-01. It is used to treat nausea and vomiting in the USA.
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Clinical
Drug
Target
Variants
Financial
Trends
Safety
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5D
1M
3M
6M
YTD
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2Y
5Y
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FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
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Primary completion date
Completion date
Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
signs and symptoms pathological conditionsD013568
Trade Name
FDA
EMA
Tigan, Trimethobenzamide (discontinued: Tigan, Trimethobenzamide)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Trimethobenzamide hydrochloride
Tradename
Company
Number
Date
Products
TIGANEndoN-017530 RX1982-01-01
1 products, RLD, RS
Show 1 discontinued
Labels
FDA
EMA
Brand Name
Status
Last Update
tiganNew Drug Application2026-03-10
tigan(r) (trimethobenzamide hydrochloride)New Drug Application2024-01-28
trimethobenzamideANDA2023-01-12
trimethobenzamide hydrochlorideANDA2025-12-11
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
vomiting—D014839R11.1
nausea—D009325R11.0
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
R: Respiratory system drugs
— R06: Antihistamines for systemic use
— R06A: Antihistamines for systemic use
— R06AA: Aminoalkyl ethers, systemic antihistamines
— R06AA10: Trimethobenzamide
HCPCS
Code
Description
J3250
Injection, trimethobenzamide hcl, up to 200 mg
Q0173
Trimethobenzamide hydrochloride, 250 mg, oral, fda approved prescription anti-emetic, for use as a complete therapeutic substitute for an iv anti-emetic at the time of chemotherapy treatment, not to exceed a 48 hour dosage regimen
Clinical
Clinical Trials
9 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Parkinson diseaseD010300EFO_0002508G201——2—3
InfertilityD007246EFO_0000545————1—1
Motor disordersD000068079—————1—1
VomitingD014839—R11.1———1—1
NauseaD009325—R11.0———1—1
Indications Phases 3
No data
Indications Phases 2
No data
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients———1————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
HyperkinesisD006948——————11
Attention deficit disorder with hyperactivityD001289EFO_0003888F90————11
MyopiaD009216EFO_0003927H52.1————11
Refractive errorsD012030HP_0000483H52.7————11
Myocardial infarctionD009203EFO_0000612I21————11
Acute coronary syndromeD054058EFO_0005672—————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameTrimethobenzamide
INNtrimethobenzamide
Description
Trimethobenzamide is the amide obtained by formal condensation of 3,4,5-trihydroxybenzoic acid with 4-[2-(N,N-dimethylamino)ethoxy]benzylamine. It is used to prevent nausea and vomitting in humans. It has a role as an antiemetic. It is a tertiary amino compound and a member of benzamides.
Classification
Small molecule
Drug class—
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Structure (InChI/SMILES or Protein Sequence)
COc1cc(C(=O)NCc2ccc(OCCN(C)C)cc2)cc(OC)c1OC
Identifiers
PDB—
CAS-ID138-56-7
RxCUI—
ChEMBL IDCHEMBL1201256
ChEBI ID27796
PubChem CID5577
DrugBankDB00662
UNII IDW2X096QY97 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
No data
Estimated US medical usage
Trimethobenzamide
+
Benzocaine
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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Trimethobenzamide
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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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 275 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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174 adverse events reported
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