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United States · US · US:71335-0801_645edeba-9a73-4d0a-ac84-2de98e89b760
bupropion
Orange BookUNIISPLATC N06AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc11713350801160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-1)
- ndc117133508012180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-2)
- ndc11713350801330 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-3)
- ndc11713350801490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-4)
- ndc117133508015120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-5)
- ndc11713350801628 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-6)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A202304
AB1AB1AB1
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": {
"cefaaa17-f79a-4ba6-8f97-a59f60e07b75": {
"match": "brand_token",
"title": "BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]",
"spl_version": "105",
"published_date": "2026-06-01"
}
},
"productid": "71335-0801_645edeba-9a73-4d0a-ac84-2de98e89b760",
"productndc": "71335-0801",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "202304",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "100MG",
"product_no": "001",
"approval_date": "May 26, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "150MG",
"product_no": "002",
"approval_date": "May 26, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "200MG",
"product_no": "003",
"approval_date": "May 26, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUPROPION HYDROCHLORIDE",
"proprietary_name": "bupropion",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202304",
"marketing_category": "ANDA",
"nonproprietary_name": "bupropion hydrochloride",
"start_marketing_date": "20141101",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code N06AX12.
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