Gatifloxacin
Zymaxid (gatifloxacin) is a small molecule pharmaceutical. Gatifloxacin was first approved as Zymar on 2003-03-28. It is used to treat bacterial conjunctivitis, bacterial infections, bacterial pneumonia, bronchitis, and cystitis amongst others in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
infections | D007239 |
respiratory tract diseases | D012140 |
otorhinolaryngologic diseases | D010038 |
eye diseases | D005128 |
urogenital diseases | D000091642 |
Trade Name
FDA
EMA
Zymaxid (generic drugs available since 2013-08-28, discontinued: Zymar)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Gatifloxacin
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
ZYMAXID | AbbVie | N-022548 RX | 2010-05-18 | 1 products, RLD, RS |
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Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
gatifloxacin | NDA authorized generic | 2016-09-01 |
zymaxid | New Drug Application | 2016-09-05 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
bacterial conjunctivitis | EFO_1000829 | D003234 | H10.0 |
bacterial infections | — | D001424 | A49 |
bacterial pneumonia | EFO_1001272 | D018410 | J15.9 |
bronchitis | — | D001991 | J40 |
cystitis | EFO_1000025 | D003556 | N30 |
escherichia coli infections | EFO_1001318 | D004927 | B96.20 |
gonorrhea | DOID_7551 | D006069 | A54 |
haemophilus infections | EFO_1001127 | D006192 | — |
klebsiella infections | EFO_1001353 | D007710 | — |
proteus infections | EFO_1001130 | D011512 | — |
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Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
J: Antiinfectives for systemic use
— J01: Antibacterials for systemic use
— J01M: Quinolone antibacterials
— J01MA: Fluoroquinolone antibacterials, systemic
— J01MA16: Gatifloxacin
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01A: Antiinfective ophthalmologics
— S01AE: Fluoroquinolone antiinfectives, ophthalmologic
— S01AE06: Gatifloxacin
HCPCS
No data
Clinical
Clinical Trials
3 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Pathologic processes | D010335 | — | — | — | 1 | — | 1 |
Indications Phases 3
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Brain diseases | D001927 | HP_0001298 | G93.40 | — | 1 | — | — | — | 1 |
Spinal cord diseases | D013118 | HP_0002196 | G95.9 | — | 1 | — | — | — | 1 |
Indications Phases 1
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | GATIFLOXACIN |
INN | gatifloxacin |
Description | Gatifloxacin is a monocarboxylic acid that is 4-oxo-1,4-dihydroquinoline-3-carboxylic acid which is substituted on the nitrogen by a cyclopropyl group and at positions 6, 7, and 8 by fluoro, 3-methylpiperazin-1-yl, and methoxy groups, respectively. Gatifloxacin is an antibiotic of the fourth-generation fluoroquinolone family, that like other members of that family, inhibits the bacterial topoisomerase type-II enzymes. It has a role as an antiinfective agent, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor and an antimicrobial agent. It is a quinolinemonocarboxylic acid, a N-arylpiperazine, an organofluorine compound, a quinolone and a quinolone antibiotic. |
Classification | Small molecule |
Drug class | antibacterials (quinolone derivatives) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | COc1c(N2CCNC(C)C2)c(F)cc2c(=O)c(C(=O)O)cn(C3CC3)c12 |
Identifiers
PDB | — |
CAS-ID | 112811-59-3 |
RxCUI | 1546025 |
ChEMBL ID | CHEMBL31 |
ChEBI ID | 5280 |
PubChem CID | 5379 |
DrugBank | DB01044 |
UNII ID | 81485Y3A9A (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 5,007 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3,024 adverse events reported
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