Moxifloxacin
Moxifloxacin Hydrochloride is a generic antibiotic tablet used to treat certain bacterial infections. Each film-coated tablet contains 400 mg of moxifloxacin hydrochloride and is taken orally. Manufactured by Dr. Reddy's Laboratories Limited under ANDA 076938, it's available in prescription form. This information was generated using AI and is provided for informational and research purposes only.
Complete Metadata
| @type | dcat:Dataset |
|---|---|
| accessLevel | public |
| accrualPeriodicity | R/P1Y |
| bureauCode |
[
"009:10"
]
|
| contactPoint |
{
"fn": "Division of Drug Information",
"@type": "vcard:Contact",
"hasEmail": "mailto:druginfo@fda.hhs.gov"
}
|
| description | Moxifloxacin Hydrochloride is a generic antibiotic tablet used to treat certain bacterial infections. Each film-coated tablet contains 400 mg of moxifloxacin hydrochloride and is taken orally. Manufactured by Dr. Reddy's Laboratories Limited under ANDA 076938, it's available in prescription form. This information was generated using AI and is provided for informational and research purposes only. |
| distribution |
[
{
"@type": "dcat:Distribution",
"title": "Moxifloxacin",
"mediaType": "text/html",
"description": "
Access the FDA dataset for Moxifloxacin — ANDA 206242 submitted by Mylan Institutional LLC
",
"downloadURL": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=206242"
}
]
|
| identifier | ANDA206242 |
| issued | 2016-09-16 |
| keyword |
[
"drug-manufacturers",
"drug-safety",
"medications",
"prescription-drugs",
"public-health"
]
|
| landingPage | https://www.fda.gov/drugs |
| license | https://open.fda.gov/license |
| modified | 2025-03-17 |
| programCode |
[
"009:002"
]
|
| publisher |
{
"name": "U.S. Food and Drug Administration",
"@type": "org:Organization"
}
|
| theme |
[
"FDA"
]
|
| title | Moxifloxacin |
