{
"NDC": {
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"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-717-01) > 1 TABLET in 1 BLISTER PACK (68084-717-11) ",
"NDC11Code": "68084-0717-01",
"ProductNDC": "68084-717",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ranitidine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ranitidine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20140725",
"EndMarketingDate": "20180930",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077824",
"LabelerName": "American Health Packaging",
"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": "2018-10-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140725",
"EndMarketingDatePackage": "20180930",
"SamplePackage": "N"
}
}