10702-238-50 : NDC 2026 Code

10702-238-50 : Oxycodone And Acetaminophen ( Oxycodone And Acetaminophen )

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NDC Code : 10702-238-50 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "10702-238-50",
    "PackageDescription": "500 mL in 1 BOTTLE (10702-238-50) ",
    "NDC11Code": "10702-0238-50",
    "ProductNDC": "10702-238",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Oxycodone And Acetaminophen",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Oxycodone And Acetaminophen",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20191205",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211499",
    "LabelerName": "KVK-Tech, Inc.",
    "SubstanceName": "ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE",
    "StrengthNumber": "325; 5",
    "StrengthUnit": "mg/5mL; mg/5mL",
    "Pharm_Classes": "Full Opioid Agonists [MoA], Opioid Agonist [EPC]",
    "DEASchedule": "CII",
    "Status": "Active",
    "LastUpdate": "2024-03-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20191205",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}