{
"NDC": {
"NDCCode": "17856-0386-1",
"PackageDescription": "72 CUP in 1 CASE (17856-0386-1) / 5 mL in 1 CUP (17856-0386-2) ",
"NDC11Code": "17856-0386-01",
"ProductNDC": "17856-0386",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydromorphone Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Hydromorphone Hydrochloride",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20120301",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074653",
"LabelerName": "ATLANTIC BIOLOGICALS CORP.",
"SubstanceName": "HYDROMORPHONE HYDROCHLORIDE",
"StrengthNumber": "1",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Full Opioid Agonists [MoA], Opioid Agonist [EPC]",
"DEASchedule": "CII",
"Status": "Deprecated",
"LastUpdate": "2026-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20240515",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}