70069-081-01 : NDC 2026 Code

70069-081-01 : Moxifloxacin Hydrochloride ( Moxifloxacin Hydrochloride )

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NDC Code : 70069-081-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70069-081-01",
    "PackageDescription": "1 BOTTLE in 1 CARTON (70069-081-01)  / 3 mL in 1 BOTTLE",
    "NDC11Code": "70069-0081-01",
    "ProductNDC": "70069-081",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Moxifloxacin Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Moxifloxacin Hydrochloride",
    "DosageFormName": "SOLUTION/ DROPS",
    "RouteName": "OPHTHALMIC",
    "StartMarketingDate": "20241125",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA209698",
    "LabelerName": "Somerset Therapeutics, LLC",
    "SubstanceName": "MOXIFLOXACIN HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-11-30",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241125",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}