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United States · US · US:0187-0731_22308f71-fc56-430d-b559-bed47e17a46c
WELLBUTRIN
Orange BookUNIISPLATC N06AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBausch Health US LLC
CountryUS (United States)
ATC codeN06AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1101870731077 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-07)
- ndc11018707313030 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-30)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
N021515
AB3AB3
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ZG7E5POY8O",
"rxcui": "203204",
"inchikey": "HEYVINCGKDONRU-UHFFFAOYSA-N",
"display_name": "BUPROPION HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"cbc8c074-f080-4489-a5ae-207b5fadeba3": {
"match": "brand_token",
"title": "WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]",
"spl_version": "39",
"published_date": "2026-04-30"
}
},
"productid": "0187-0731_22308f71-fc56-430d-b559-bed47e17a46c",
"productndc": "0187-0731",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "021515",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB3",
"strength": "150MG",
"product_no": "001",
"approval_date": "Aug 28, 2003"
},
{
"rs": true,
"rld": true,
"te_code": "AB3",
"strength": "300MG",
"product_no": "002",
"approval_date": "Aug 28, 2003"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUPROPION HYDROCHLORIDE",
"proprietary_name": "WELLBUTRIN",
"active_ingred_unit": "mg/1",
"application_number": "NDA021515",
"marketing_category": "NDA",
"nonproprietary_name": "bupropion hydrochloride",
"start_marketing_date": "20030829",
"active_numerator_strength": "300"
}Related drugs
Other records sharing ATC code N06AX12.
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