55700-884-10 : NDC 2026 Code

55700-884-10 : Ciprofloxacin Hydrochloride ( Ciprofloxacin )

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NDC Code : 55700-884-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "55700-884-10",
    "PackageDescription": "10 TABLET, FILM COATED in 1 BOTTLE (55700-884-10) ",
    "NDC11Code": "55700-0884-10",
    "ProductNDC": "55700-884",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ciprofloxacin",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ciprofloxacin Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20201006",
    "EndMarketingDate": "20250131",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077859",
    "LabelerName": "Quality Care Products, LLC",
    "SubstanceName": "CIPROFLOXACIN HYDROCHLORIDE",
    "StrengthNumber": "250",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-02-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20201207",
    "EndMarketingDatePackage": "20250131",
    "SamplePackage": "N"
  }
}