{
"NDC": {
"NDCCode": "59368-225-02",
"PackageDescription": "500 TABLET in 1 BOTTLE (59368-225-02) ",
"NDC11Code": "59368-0225-02",
"ProductNDC": "59368-225",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Sunmark Pain Reliever",
"ProprietaryNameSuffix": "Extra Strength",
"NonProprietaryName": "Acetaminophen",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20030811",
"EndMarketingDate": "20250601",
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M013",
"LabelerName": "Praxis, LLC",
"SubstanceName": "ACETAMINOPHEN",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-06-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20030811",
"EndMarketingDatePackage": "20250601",
"SamplePackage": "N"
}
}