66689-711-30 : NDC 2026 Code

66689-711-30 : Methadone Hydrochloride ( Methadone Hydrochloride )

Additionally :

You can get information about “66689-711-30” NDC code in 66689-711-30 in HTML format

HTML | 66689-711-30 in TXT (Plain Text) format

TXT | 66689-711-30 in PDF (Portable Document Format)

PDF | 66689-711-30 in XML format

XML formats.

NDC Code : 66689-711-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "66689-711-30",
    "PackageDescription": "3 TRAY in 1 CASE (66689-711-30)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (66689-711-05) ",
    "NDC11Code": "66689-0711-30",
    "ProductNDC": "66689-711",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Methadone Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Methadone Hydrochloride",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100801",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090707",
    "LabelerName": "VistaPharm, LLC",
    "SubstanceName": "METHADONE HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/5mL",
    "Pharm_Classes": "Full Opioid Agonists [MoA], Opioid Agonist [EPC]",
    "DEASchedule": "CII",
    "Status": "Active",
    "LastUpdate": "2026-03-31",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260320",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}