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United States · US · US:11673-604_5bfbc5ad-0e3e-4469-b42f-d5ee940534cf
up and up ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1111673604781 BOTTLE in 1 CARTON (11673-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
- ndc111167360490500 TABLET, FILM COATED in 1 BOTTLE (11673-604-90)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A072096
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WK2XYI10QM",
"rxcui": "5640",
"inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
"display_name": "IBUPROFEN",
"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": "11673-604_5bfbc5ad-0e3e-4469-b42f-d5ee940534cf",
"productndc": "11673-604",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "072096",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Dec 8, 1987"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "up and up ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072096",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20090528",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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