68682-582-30 : NDC 2026 Code

68682-582-30 : Bupropion Hydrobromide ( Bupropion Hydrobromide )

Additionally :

You can get information about “68682-582-30” NDC code in 68682-582-30 in HTML format

HTML | 68682-582-30 in TXT (Plain Text) format

TXT | 68682-582-30 in PDF (Portable Document Format)

PDF | 68682-582-30 in XML format

XML formats.

NDC Code : 68682-582-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68682-582-30",
    "PackageDescription": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-582-30) ",
    "NDC11Code": "68682-0582-30",
    "ProductNDC": "68682-582",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrobromide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrobromide",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260629",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA022108",
    "LabelerName": "Oceanside Pharmaceuticals",
    "SubstanceName": "BUPROPION HYDROBROMIDE",
    "StrengthNumber": "522",
    "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": "Active",
    "LastUpdate": "2026-06-30",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20260629",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}