76413-317-30 : NDC 2026 Code

76413-317-30 : Ranitidine ( Zantac )

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NDC Code : 76413-317-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "76413-317-30",
    "PackageDescription": "3 BLISTER PACK in 1 CARTON (76413-317-30)  &gt; 10 TABLET, COATED in 1 BLISTER PACK",
    "NDC11Code": "76413-0317-30",
    "ProductNDC": "76413-317",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Zantac",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ranitidine",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20061221",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA020520",
    "LabelerName": "Central Texas Community Health Centers",
    "SubstanceName": "RANITIDINE HYDROCHLORIDE",
    "StrengthNumber": "75",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20061221",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}