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United States · US · US:85237-1786_3ca7531b-364f-d68e-e063-6294a90a3ded
ADVIL
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSelect Consumer Group
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1185237178611 POUCH in 1 BLISTER PACK (85237-1786-1) / 1 TABLET, COATED in 1 POUCH
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
N018989
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": {
"a3c30dd2-75f3-4f8b-88d7-4a63dea5bad7": {
"match": "brand_token",
"title": "ADVIL PM (DIPHENHYDRAMINE CITRATE, IBUPROFEN) TABLET, COATED [NAVAJO MANUFACTURING COMPANY INC.]",
"spl_version": "3",
"published_date": "2026-04-09"
}
},
"productid": "85237-1786_3ca7531b-364f-d68e-e063-6294a90a3ded",
"productndc": "85237-1786",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "018989",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "May 18, 1984"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "ADVIL",
"active_ingred_unit": "mg/1",
"application_number": "NDA018989",
"marketing_category": "NDA",
"nonproprietary_name": "ibuprofen",
"start_marketing_date": "19840518",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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