70518-3551-0 : NDC 2025 Code

70518-3551-0 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

Additionally :

You can get information about “70518-3551-0” NDC code in 70518-3551-0 in HTML format

HTML | 70518-3551-0 in TXT (Plain Text) format

TXT | 70518-3551-0 in PDF (Portable Document Format)

PDF | 70518-3551-0 in XML format

XML formats.

NDC Code : 70518-3551-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-3551-0",
    "PackageDescription": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3551-0) ",
    "NDC11Code": "70518-3551-00",
    "ProductNDC": "70518-3551",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221007",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078866",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "150",
    "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": "2024-10-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20221007",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}