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United States · US · US:24979-247_96a5dcb3-5d09-4357-96e3-8005ef094b2c
Forfivo
Orange BookUNIISPLATC N06AX12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUpsher-Smith Laboratories, LLC
CountryUS (United States)
ATC codeN06AX12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11249792470630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)
Annotations
UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
N022497
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": {
"80b01182-dc94-4990-8ebb-55c306d7e536": {
"match": "brand_token",
"title": "FORFIVO XL (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [UPSHER-SMITH LABORATORIES, LLC]",
"spl_version": "8",
"published_date": "2025-12-08"
}
},
"productid": "24979-247_96a5dcb3-5d09-4357-96e3-8005ef094b2c",
"productndc": "24979-247",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "022497",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "450MG",
"product_no": "001",
"approval_date": "Nov 10, 2011"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BUPROPION HYDROCHLORIDE",
"proprietary_name": "Forfivo",
"active_ingred_unit": "mg/1",
"application_number": "NDA022497",
"marketing_category": "NDA",
"nonproprietary_name": "bupropion hydrochloride",
"start_marketing_date": "20231215",
"active_numerator_strength": "450"
}Related drugs
Other records sharing ATC code N06AX12.
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