73473-903-30 : NDC 2026 Code

73473-903-30 : Moxifloxacin Hydrochloride ( Moxifloxacin )

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NDC Code : 73473-903-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "73473-903-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30) ",
    "NDC11Code": "73473-0903-30",
    "ProductNDC": "73473-903",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Moxifloxacin",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Moxifloxacin Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20251212",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA206295",
    "LabelerName": "Solaris Pharma Corporation",
    "SubstanceName": "MOXIFLOXACIN HYDROCHLORIDE",
    "StrengthNumber": "400",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251212",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}