{
"NDC": {
"NDCCode": "70756-830-16",
"PackageDescription": "16000 TABLET, EXTENDED RELEASE in 1 BOX (70756-830-16) ",
"NDC11Code": "70756-0830-16",
"ProductNDC": "70756-830",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Bupropion Hcl Er (xl)",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Bupropion Hcl Er",
"DosageFormName": "TABLET, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20260501",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA022497",
"LabelerName": "Lifestar Pharma LLC",
"SubstanceName": "BUPROPION HYDROCHLORIDE",
"StrengthNumber": "450",
"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": "2026-05-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260501",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}