70934-017-04 : NDC 2026 Code

70934-017-04 : Ranitidine ( Ranitidine )

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NDC Code : 70934-017-04 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-017-04",
    "PackageDescription": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-04) ",
    "NDC11Code": "70934-0017-04",
    "ProductNDC": "70934-017",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ranitidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ranitidine",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20181025",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078542",
    "LabelerName": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals",
    "SubstanceName": "RANITIDINE HYDROCHLORIDE",
    "StrengthNumber": "150",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-05-07",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20190603",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}