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United States · US · US:0363-0291_93d5e52b-b346-422b-b801-25ce2a20888b
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWalgreen Company
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11036302910310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-03)
- ndc110363029114500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-14)
- ndc1103630291161000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-16)
- ndc110363029129150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-29)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075010
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": {
"aeee629b-255c-40d8-8e95-779aec00f723": {
"match": "brand_token",
"title": "IBUPROFEN TABLET [NORTHSTAR RX LLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "0363-0291_93d5e52b-b346-422b-b801-25ce2a20888b",
"productndc": "0363-0291",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075010",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 1, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075010",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "19880524",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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