62559-758-04 : NDC 2026 Code

62559-758-04 : Promethazine Hydrochloride And Dextromethorphan Hydrobromide ( Promethazine Hydrochloride And Dextromethorphan Hydrobromide )

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NDC Code : 62559-758-04 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "62559-758-04",
    "PackageDescription": "118 mL in 1 BOTTLE (62559-758-04) ",
    "NDC11Code": "62559-0758-04",
    "ProductNDC": "62559-758",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Promethazine Hydrochloride And Dextromethorphan Hydrobromide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Promethazine Hydrochloride And Dextromethorphan Hydrobromide",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240905",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA011265",
    "LabelerName": "ANI Pharmaceuticals, Inc.",
    "SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE",
    "StrengthNumber": "15; 6.25",
    "StrengthUnit": "mg/5mL; mg/5mL",
    "Pharm_Classes": "Phenothiazine [EPC], Phenothiazines [CS], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-08-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240905",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}