60432-604-04 : NDC 2026 Code

60432-604-04 : Dextromethorphan Hydrobromide And Promethazine Hydrochloride ( Dextromethorphan Hydrobromide And Promethazine Hydrochloride )

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NDC Code : 60432-604-04 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60432-604-04",
    "PackageDescription": "118 mL in 1 BOTTLE, PLASTIC (60432-604-04)",
    "NDC11Code": "60432-0604-04",
    "ProductNDC": "60432-604",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Dextromethorphan Hydrobromide And Promethazine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Dextromethorphan Hydrobromide And Promethazine Hydrochloride",
    "DosageFormName": "SYRUP",
    "RouteName": "ORAL",
    "StartMarketingDate": "19850104",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA088864",
    "LabelerName": "Morton Grove Pharmaceuticals, Inc.",
    "SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE",
    "StrengthNumber": "15; 6.25",
    "StrengthUnit": "mg/5mL; mg/5mL",
    "Pharm_Classes": "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-07-27",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}