{
"NDC": {
"NDCCode": "68163-066-24",
"PackageDescription": "24 TABLET, FILM COATED in 1 CARTON (68163-066-24) ",
"NDC11Code": "68163-0066-24",
"ProductNDC": "68163-066",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Drx Choice",
"ProprietaryNameSuffix": "Extra Strength Headache Relief",
"NonProprietaryName": "Acetaminophen, Aspirin (nsaid), Caffeine",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20260814",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M013",
"LabelerName": "Raritan Pharmaceuticals Inc.",
"SubstanceName": "ACETAMINOPHEN; ASPIRIN; CAFFEINE",
"StrengthNumber": "250; 250; 65",
"StrengthUnit": "mg/1; mg/1; mg/1",
"Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-09-15",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260814",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}