48102-018-30 : NDC 2026 Code

48102-018-30 : Moxifloxacin Hydrochloride ( Moxifloxacin Hydrochloride )

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NDC Code : 48102-018-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "48102-018-30",
    "PackageDescription": "30 TABLET in 1 BOTTLE (48102-018-30)",
    "NDC11Code": "48102-0018-30",
    "ProductNDC": "48102-018",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Moxifloxacin Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Moxifloxacin Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160122",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA205348",
    "LabelerName": "Fera Pharmaceuticals, LLC",
    "SubstanceName": "MOXIFLOXACIN HYDROCHLORIDE",
    "StrengthNumber": "400",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2016-12-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}