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Drug ReportsBepotastine besylate
Bepotastine besylate
Bepotastine, Bepreve (bepotastine besylate) is a small molecule pharmaceutical. Bepotastine besylate was first approved as Bepreve on 2009-09-08.
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Brand Name
Status
Last Update
bepotastine besilateANDA2024-10-10
bepotastine besilate ophthalmic solution 1.5%ANDA2023-07-21
bepreveNew Drug Application2022-08-31
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FDA Information
Bepotastine Besilate, Bepreve, Bausch And Lomb Inc
87847892025-01-13DP
87847892025-01-13DP
87847892025-01-13DP
87847892025-01-13DP
ATC Codes
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Clinical
Clinical Trials
30 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
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ConjunctivitisD003231H1023217
Allergic conjunctivitisD003233EFO_0007141H10.4423217
Indications Phases 3
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Indications Phases 2
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Ontology
ICD-10
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Allergic rhinitisD065631J30.9144
RhinitisD012220EFO_0008521J31144
Allergic rhinitis seasonalD006255EFO_0003956J30144
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 nameBepotastine besylate
INN_
Description
Bepotastine (Talion, Bepreve) is a 2nd generation antihistamine. It was approved in Japan for use in the treatment of allergic rhinitis and urticaria/pruritus in July 2000, and January 2002, respectively. It is marketed in the United States as an eye drop under the brand name Bepreve, by ISTA Pharmaceuticals, a subsidiary of Bausch + Lomb.
Classification
Small molecule
Drug classantihistaminics (histamine-H1 receptor antagonists)
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Structure (InChI/SMILES or Protein Sequence)
O=C(O)CCCN1CCC(O[C@@H](c2ccc(Cl)cc2)c2ccccn2)CC1.O=S(=O)(O)c1ccccc1
Identifiers
PDB
CAS-ID190786-44-8
RxCUI
ChEMBL IDCHEMBL1201759
ChEBI ID31281
PubChem CID2350
DrugBankDB04890
UNII ID6W18MO1QR3 (ChemIDplus, GSRS)
Target
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Variants
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Financial
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Trends
PubMed Central
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Additional graphs summarizing 159 documents
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Safety
Black-box Warning
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Adverse Events
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369 adverse events reported
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