52125-508-02 : NDC 2026 Code

52125-508-02 : Bupropion Hydrochloride ( Bupropion Hydrochloridexl )

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NDC Code : 52125-508-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "52125-508-02",
    "PackageDescription": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 VIAL (52125-508-02)",
    "NDC11Code": "52125-0508-02",
    "ProductNDC": "52125-508",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloridexl",
    "ProprietaryNameSuffix": "Xl",
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20130603",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077715",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "300",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2016-12-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}