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Drug ReportsOxcarbazepine
Oxcarbazepine
Oxcarbazepine, Oxtellar, Trileptal (oxcarbazepine) is a small molecule pharmaceutical. Oxcarbazepine was first approved as Trileptal on 2000-01-14. It is used to treat epilepsy and partial epilepsies in the USA.
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Drug
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Trends
Safety
Events Timeline
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6M
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1Y
2Y
5Y
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FDA approval date
EMA approval date
Patent expiration date
Study first post date
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Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
nervous system diseasesD009422
Trade Name
FDA
EMA
Oxcarbazepine, Oxtellar, Trileptal (discontinued: Oxcarbazepine)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Oxcarbazepine
Tradename
Company
Number
Date
Products
TRILEPTALNovartisN-021014 RX2000-01-14
3 products, RLD, RS
TRILEPTALNovartisN-021285 RX2001-05-25
1 products, RLD, RS
OXTELLAR XRSupernus PharmaceuticalsN-202810 RX2012-10-19
3 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
oxcarbazepineANDA2024-10-30
oxtellar xrNew Drug Application2024-10-10
trileptalNew Drug Application2024-07-23
Indications
FDA
EMA
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Oxcarbazepine, Oxtellar Xr, Supernus Pharms
77228982027-04-13DP
79101312027-04-13U-2041
86176002027-04-13DP
88219302027-04-13DP
91197912027-04-13U-2041
93519752027-04-13DP
93705252027-04-13DP
98552782027-04-13DP
102200422027-04-13U-2501
111669602027-04-13DP
118965992027-04-13DP
ATC Codes
N: Nervous system drugs
N03: Antiepileptics
N03A: Antiepileptics
N03AF: Carboxamide derivatives, antiepileptics
N03AF02: Oxcarbazepine
HCPCS
No data
Clinical
Clinical Trials
67 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
EpilepsyD004827EFO_0000474G40.96681131
Partial epilepsiesD004828EFO_000426325512
SeizuresD012640HP_0002069G40.42233311
NeuralgiaD009437EFO_00094301416
Bipolar disorderD001714EFO_0000289F30.9415
Trigeminal neuralgiaD014277EFO_1001219G50.0213
DepressionD003863F33.9112
AggressionD000374EFO_0003015112
Drug resistant epilepsyD00006927922
Metabolic clearance rateD00865711
Show 11 more
Indications Phases 3
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Central nervous system neoplasmsD016543122
Nervous system neoplasmsD009423122
Multiple sclerosisD009103EFO_0003885G35112
SclerosisD012598112
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients235
GlioblastomaD005909EFO_000051533
GliomaD005910EFO_000052033
GliosarcomaD01831633
AstrocytomaD001254EFO_000027133
OligodendrogliomaD009837EFO_000063111
NeoplasmsD009369C8011
Cancer painD000072716G89.311
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameOxcarbazepine
INNoxcarbazepine
Description
Oxcarbazepine is a dibenzoazepine derivative, having a carbamoyl group at the ring nitrogen, substituted with an oxo group at C-4 of the azepeine ring which is also hydrogenated at C-4 and C-5. It is a anticholinergic anticonvulsant and mood stabilizing drug, used primarily in the treatment of epilepsy. It has a role as an anticonvulsant and a drug allergen. It is a dibenzoazepine and a cyclic ketone. It contains a carbamoyl group.
Classification
Small molecule
Drug classtricyclic compounds
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
NC(=O)N1c2ccccc2CC(=O)c2ccccc21
Identifiers
PDB
CAS-ID28721-07-5
RxCUI
ChEMBL IDCHEMBL1068
ChEBI ID7824
PubChem CID34312
DrugBankDB00776
UNII IDVZI5B1W380 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
Oxtellar Supernus Pharmaceuticals
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Estimated US medical usage
Oxcarbazepine
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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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 8,039 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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16,442 adverse events reported
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