50383-959-10 : NDC 2026 Code

50383-959-10 : Protriptyline Hydrochloride ( Protriptyline Hydrochloride )

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NDC Code : 50383-959-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50383-959-10",
    "PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (50383-959-10) ",
    "NDC11Code": "50383-0959-10",
    "ProductNDC": "50383-959",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Protriptyline Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Protriptyline Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20131028",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202220",
    "LabelerName": "Hi-Tech Pharmacal Co., Inc.",
    "SubstanceName": "PROTRIPTYLINE HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Tricyclic Antidepressant [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-11-17",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20131028",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}