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United States · US · US:50090-7112_732484bd-0f31-4406-8429-dc70c3a570d0
Bupropion Hydrochloride
Orange BookUNIISPLATC N06AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeN06AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500907112090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7112-0)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A210015
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": "50090-7112_732484bd-0f31-4406-8429-dc70c3a570d0",
"productndc": "50090-7112",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "210015",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB3",
"strength": "150MG",
"product_no": "001",
"approval_date": "Jun 14, 2018"
},
{
"rs": false,
"rld": false,
"te_code": "AB3",
"strength": "300MG",
"product_no": "002",
"approval_date": "Jun 14, 2018"
}
],
"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": "ANDA210015",
"marketing_category": "ANDA",
"nonproprietary_name": "bupropion hydrochloride",
"start_marketing_date": "20230430",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code N06AX12.
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