70518-4312-0 : NDC 2026 Code

70518-4312-0 : Moxifloxacin Hydrochloride Tablets, 400 Mg ( Moxifloxacin Hydrochloride Tablets, 400 Mg )

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NDC Code : 70518-4312-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-4312-0",
    "PackageDescription": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0) ",
    "NDC11Code": "70518-4312-00",
    "ProductNDC": "70518-4312",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Moxifloxacin Hydrochloride Tablets, 400 Mg",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Moxifloxacin Hydrochloride Tablets, 400 Mg",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250318",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA208682",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE",
    "StrengthNumber": "400",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-10-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250318",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}