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Drug ReportsMoxifloxacin
Moxifloxacin
Moxifloxacin, Vigamox (moxifloxacin) is a small molecule pharmaceutical. Moxifloxacin was first approved as Avelox on 1999-12-10. It is used to treat bacterial infections, bacterial pneumonia, bacteroides infections, bronchitis, and cystitis amongst others in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
respiratory tract diseasesD012140
otorhinolaryngologic diseasesD010038
urogenital diseasesD000091642
Trade Name
FDA
EMA
Moxifloxacin, Vigamox (discontinued: Avelox, Moxeza, Moxifloxacin)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Moxifloxacin hydrochloride
Tradename
Company
Number
Date
Products
MOXIFLOXACIN HYDROCHLORIDEFresenius KabiN-205572 RX2015-04-03
1 products, RLD, RS
VIGAMOXHarrowN-021598 RX2003-04-15
1 products, RLD, RS
Show 3 discontinued
Labels
FDA
EMA
Brand Name
Status
Last Update
aveloxNew Drug Application2011-12-13
avelox abc packNew Drug Application2009-10-25
dex-moxiunapproved drug other2020-02-10
dex-moxi pfunapproved drug other2018-05-08
dex-moxi-ketorunapproved drug other2020-02-10
dexmoxiketor pfunapproved drug other2018-05-08
ixoba munapproved drug other2021-11-03
moxezaNew Drug Application2021-08-11
moxifloxacinANDA2024-12-31
moxifloxacin hydrochlorideANDA2025-01-07
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Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
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FDA Information
Moxifloxacin Hydrochloride, Moxeza, Harrow Eye
84503112029-05-29DP
91141682029-05-29DP
ATC Codes
J: Antiinfectives for systemic use
— J01: Antibacterials for systemic use
— J01M: Quinolone antibacterials
— J01MA: Fluoroquinolone antibacterials, systemic
— J01MA14: Moxifloxacin
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01A: Antiinfective ophthalmologics
— S01AE: Fluoroquinolone antiinfectives, ophthalmologic
— S01AE07: Moxifloxacin
HCPCS
Code
Description
J2280
Injection, moxifloxacin, 100 mg
J2281
Injection, moxifloxacin (fresenius kabi) not therapeutically equivalent to j2280, 100 mg
Clinical
Clinical Trials
648 clinical trials
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Indications Phases 4
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Indications Phases 3
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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
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMoxifloxacin
INNmoxifloxacin
Description
Moxifloxacin is a quinolone that consists of 4-oxo-1,4-dihydroquinoline-3-carboxylic acid bearing a cyclopropyl substituent at position 1, a fluoro substitiuent at position 6, a (4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl group at position 7 and a methoxy substituent at position 8. A member of the fluoroquinolone class of antibacterial agents. It has a role as an antibacterial drug. It is a quinolinemonocarboxylic acid, a quinolone, a member of cyclopropanes, a pyrrolidinopiperidine, an aromatic ether, a quinolone antibiotic and a fluoroquinolone antibiotic. It is a conjugate base of a moxifloxacinium(1+).
Classification
Small molecule
Drug classantibacterials (quinolone derivatives)
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
COc1c(N2C[C@@H]3CCCN[C@@H]3C2)c(F)cc2c(=O)c(C(=O)O)cn(C3CC3)c12
Identifiers
PDB—
CAS-ID151096-09-2
RxCUI—
ChEMBL IDCHEMBL32
ChEBI ID63611
PubChem CID152946
DrugBankDB00218
UNII IDU188XYD42P (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
€
£
â‚£
No data
Estimated US medical usage
Moxifloxacin
+
Dexamethasone
Total medical expenditures per year (USD, in millions)
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Moxifloxacin
Total medical expenditures per year (USD, in millions)
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Number of persons purchased
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 24,523 documents
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Safety
Black-box Warning
Black-box warning for: Avelox, Avelox abc pack, Moxifloxacin hydrochloride, Moxifloxacin hydrochloride tablets, 400 mg, Trimipramine maleate
Adverse Events
Top Adverse Reactions
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30,982 adverse events reported
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