{
"NDC": {
"NDCCode": "49349-476-28",
"PackageDescription": "300 TABLET in 1 CANISTER (49349-476-28)",
"NDC11Code": "49349-0476-28",
"ProductNDC": "49349-476",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ranitidine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ranitidine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110811",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077824",
"LabelerName": "REMEDYREPACK INC.",
"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": "2017-02-17",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}