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Available in:
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Form
TABLET, FILM COATED
Dosage
400 mg/1
Route
ORAL
Storage
—
About This Product
Manufacturer
Aurobindo Pharma Limited
ATC Code
J01MA14
Source
OPENFDA_NDC
USFDA:Moxifloxacin
AU:B3
J01MA14(WHO)S01AE07(WHO)
AU:S4(Prescription only)US:℞-only
1-Cyclopropyl-7-[(1S,6S)-2,8-diazabicyclo[4.3.0]nonan-8-yl]-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid
151096-09-2Y[yes]
152946
DB00218Y
134802Y
U188XYD42P
D08237as HCl:D00874
ChEMBL32Y
070017
DTXSID3048491
Interactive image
COc1c2c(cc(c1N3C[C@@H]4CCCN[C@@H]4C3)F)c(=O)c(cn2C5CC5)C(=O)O
InChI=1S/C21H24FN3O4/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28)/t11-,16+/m0/s1YKey:FABPRXSRWADJSP-MEDUHNTESA-NY
Moxifloxacinis anantibiotic, used to treatbacterial infections,includingpneumonia,conjunctivitis,endocarditis,tuberculosis, andsinusitis.It can be given by mouth, byinjection into a vein, and as aneye drop.
Common side effects includediarrhea, dizziness, and headache.Severe side effects may include spontaneoustendon ruptures,nerve damage, and worsening ofmyasthenia gravis.Safety of use inpregnancyandbreastfeedingis unclear.Moxifloxacin is in thefluoroquinolonefamily of medications.It usuallykills bacteriaby blocking their ability to duplicateDNA.
Moxifloxacin was patented in 1988 and approved for use in the United States in 1999.It is on theWorld Health Organization's List of Essential Medicines.In 2023, it was the 237th most commonly prescribed medication in the United States, with more than one million prescriptions.
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Verified by medical editor
Dr. Ozarchuk, PharmD · April 2026
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