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Mebutamate
Dormate (mebutamate) is a small molecule pharmaceutical. Mebutamate was first approved as Dormate on 1982-01-01.
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Commercial
Therapeutic Areas
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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)
Mebutamate
Tradename
Company
Number
Date
Products
DORMATEMedpointe Pharm HlcN-017374 DISCN1982-01-01
1 products
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
N: Nervous system drugs
— N05: Psycholeptics
— N05B: Anxiolytics
— N05BC: Carbamate anxiolytics
— N05BC04: Mebutamate
HCPCS
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Clinical
Clinical Trials
4 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NarcolepsyD009290EFO_0000614G47.4—2———2
Attention deficit disorder with hyperactivityD001289EFO_0003888F90—1———1
Cocaine-related disordersD019970F14—1———1
Disorders of excessive somnolenceD006970G47.1—1———1
Indications Phases 1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMEBUTAMATE
INNmebutamate
Description
Mebutamate (Capla, Dormate) is an anxiolytic and sedative drug with antihypertensive effects of the carbamate class. It has effects comparable to those of barbiturates such as secobarbital, but is only around 1/3 the potency of secobarbital as a sedative. Side effects include dizziness and headaches.
Classification
Small molecule
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CCC(C)C(C)(COC(N)=O)COC(N)=O
Identifiers
PDB—
CAS-ID64-55-1
RxCUI—
ChEMBL IDCHEMBL1200922
ChEBI ID—
PubChem CID6151
DrugBankDB06797
UNII ID5H8F175RER (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:
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Additional graphs summarizing 40 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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33 adverse events reported
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