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United States · US · US:0472-2002_2e9a1263-be1c-4fa3-8108-0a634fec2593
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerActavis Pharma, Inc.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc110472200216473 mL in 1 BOTTLE (0472-2002-16)
- ndc1104722002941 BOTTLE in 1 CARTON (0472-2002-94) / 118 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A074978
AB
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": "0472-2002_2e9a1263-be1c-4fa3-8108-0a634fec2593",
"productndc": "0472-2002",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "074978",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "100MG/5ML",
"product_no": "001",
"approval_date": "Mar 25, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA074978",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20180716",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code G02CC01.
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