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United States · US · US:82442-532_54d01b77-2fd5-440f-a3b8-fb430c7a28d0
Up and Up Nicotine
Orange BookUNIISPLATC N07BA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeN07BA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118244253278100 BLISTER PACK in 1 CARTON (82442-532-78) / 1 GUM, CHEWING in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
6M3C89ZY6R
NICOTINE
RxCUI 7407
Orange Book
A076779
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "6M3C89ZY6R",
"rxcui": "7407",
"inchikey": "SNICXCGAKADSCV-JTQLQIEISA-N",
"display_name": "NICOTINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "82442-532_54d01b77-2fd5-440f-a3b8-fb430c7a28d0",
"productndc": "82442-532",
"dosage_form": "GUM, CHEWING",
"orange_book": {
"appl_no": "076779",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 4MG BASE",
"product_no": "001",
"approval_date": "Sep 16, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NICOTINE",
"proprietary_name": "Up and Up Nicotine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076779",
"marketing_category": "ANDA",
"nonproprietary_name": "Nicotine Polacrilex",
"start_marketing_date": "20240421",
"active_numerator_strength": "4"
}Related drugs
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