Moxifloxacin (oral)
Clinical data | |
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Pregnancy category | |
Routes of administration | Oral, IV, local (eyedrops) |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | 86 to 92% |
Protein binding | 30 to 50% |
Metabolism | Glucuronide and sulfate conjugation Cytochrome P450 system not involved |
Elimination half-life | 12 hours |
Excretion | Biliary and renal |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C21H24FN3O4 |
Molar mass | 401.431 g/mol |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Abdurahman Khalil, M.D. [2]
Overview
Moxifloxacin is a synthetic fluoroquinolone antibiotic agent. Bayer AG developed the drug (initially called BAY 12-8039) and it is marketed worldwide (as the hydrochloride) under the brand name Avelox® (in some countries also Avalox®) for oral treatment. Each tablet contains 400 mg. In most countries the drug is also available in parenteral form for intravenous infusion. Moxifloxacin is also sold in an ophthalmic solution (eye drops) under the name Vigamox® for the treatment of conjunctivitis.
Category
Fluoroquinolone, fourth generation.
US Brand Names
AVELOX®, MOXEZA®, VIGAMOX®.
FDA Package Insert
Description | Clinical Pharmacology | Microbiology | Indications and Usage | Contraindications | Warnings and Precautions | Adverse Reactions | Overdosage | Clinical Studies | Dosage and Administration | How Supplied | Labels and Packages
References
http://www.accessdata.fda.gov/drugsatfda_docs/label/2004/21277slr018,21085slr023_avelox_lbl.pdf
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