{
"NDC": {
"NDCCode": "70518-1829-2",
"PackageDescription": "30 TABLET in 1 BLISTER PACK (70518-1829-2) ",
"NDC11Code": "70518-1829-02",
"ProductNDC": "70518-1829",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sulfasalazine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sulfasalazine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20190128",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA007073",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "SULFASALAZINE",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Aminosalicylate [EPC], Aminosalicylic Acids [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-11-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20241231",
"StartMarketingDatePackage": "20200820",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}