🇺🇸
United States · US · US:11673-050_85dc1973-d04b-4c7e-a5c4-24c94a791a05
up and up ibuprofen pm
Orange BookUNIISPLATC D04AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeD04AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1111673050581 BOTTLE in 1 CARTON (11673-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE
- ndc1111673050601 BOTTLE in 1 CARTON (11673-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE
- ndc111167305082200 TABLET, FILM COATED in 1 BOTTLE (11673-050-82)
Annotations
UNII (FDA Substance ID)
4OD433S209
DIPHENHYDRAMINE CITRATE
RxCUI 82004
Orange Book
A079113
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4OD433S209",
"rxcui": "82004",
"inchikey": "SPCKHVPPRJWQRZ-UHFFFAOYSA-N",
"display_name": "DIPHENHYDRAMINE CITRATE",
"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": "11673-050_85dc1973-d04b-4c7e-a5c4-24c94a791a05",
"productndc": "11673-050",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "079113",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "38MG;200MG",
"product_no": "001",
"approval_date": "Dec 22, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE CITRATE; IBUPROFEN",
"proprietary_name": "up and up ibuprofen pm",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA079113",
"marketing_category": "ANDA",
"nonproprietary_name": "diphenhydramine citrate and ibuprofen",
"start_marketing_date": "20090710",
"active_numerator_strength": "38; 200"
}Related drugs
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