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United States · US · US:71335-2499_28a2d1e3-d88b-4312-99a9-54592acd5a27
Bupropion hydrochloride
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
- ndc11713352499130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-1)
- ndc11713352499260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-2)
- ndc11713352499390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-3)
- ndc117133524994120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-4)
- ndc1171335249958 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-5)
- ndc117133524996180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2499-6)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A215568
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": {
"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": "71335-2499_28a2d1e3-d88b-4312-99a9-54592acd5a27",
"productndc": "71335-2499",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "215568",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB3",
"strength": "150MG",
"product_no": "001",
"approval_date": "Feb 2, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB3",
"strength": "300MG",
"product_no": "002",
"approval_date": "Feb 2, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUPROPION HYDROCHLORIDE",
"proprietary_name": "Bupropion hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA215568",
"marketing_category": "ANDA",
"nonproprietary_name": "Bupropion hydrochloride",
"start_marketing_date": "20221215",
"active_numerator_strength": "300"
}Related drugs
Other records sharing ATC code N06AX12.
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