{
"NDC": {
"NDCCode": "70362-730-30",
"PackageDescription": "30 TABLET in 1 BOTTLE (70362-730-30) ",
"NDC11Code": "70362-0730-30",
"ProductNDC": "70362-730",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Dvorah",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Acetaminophen, Caffeine And Dihydrocodeine Bitartrate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20181206",
"EndMarketingDate": "20210311",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204209",
"LabelerName": "Skylar Laboratories, LLC",
"SubstanceName": "ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE",
"StrengthNumber": "325; 30; 16",
"StrengthUnit": "mg/1; mg/1; mg/1",
"Pharm_Classes": "Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE],Full Opioid Agonists [MoA],Opioid Agonist [EPC]",
"DEASchedule": "CIII",
"Status": "Deprecated",
"LastUpdate": "2021-03-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20181206",
"EndMarketingDatePackage": "20210311",
"SamplePackage": "N"
}
}