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United States · US · US:42806-413_4bde68a6-0945-b21f-e063-6394a90a3bc4
Bupropion Hydrochloride
Orange BookUNIISPLATC N06AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEpic Pharma, LLC
CountryUS (United States)
ATC codeN06AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11428064136060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A216766
AB2
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": "42806-413_4bde68a6-0945-b21f-e063-6394a90a3bc4",
"productndc": "42806-413",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "216766",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB2",
"strength": "150MG",
"product_no": "001",
"approval_date": "Jan 9, 2023"
}
],
"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": "ANDA216766",
"marketing_category": "ANDA",
"nonproprietary_name": "bupropion hydrochloride",
"start_marketing_date": "20230228",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code N06AX12.
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