70404-077-14 : NDC 2026 Code

70404-077-14 : Prednisolone Oral ( Prednisolone )

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NDC Code : 70404-077-14 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70404-077-14",
    "PackageDescription": "240 mL in 1 BOTTLE (70404-077-14) ",
    "NDC11Code": "70404-0077-14",
    "ProductNDC": "70404-077",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Prednisolone",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Prednisolone Oral",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260708",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA219509",
    "LabelerName": "Tulex Pharmaceuticals Inc",
    "SubstanceName": "PREDNISOLONE",
    "StrengthNumber": "15",
    "StrengthUnit": "mg/5mL",
    "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-07-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260708",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}