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United States · US · US:11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRITE AID CORPORATION
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11118227892024 TABLET, COATED in 1 BOTTLE (11822-7892-0)
- ndc11118227892250 TABLET, COATED in 1 BOTTLE (11822-7892-2)
- ndc111182278925100 TABLET, COATED in 1 BOTTLE (11822-7892-5)
- ndc111182278927200 TABLET, COATED in 1 BOTTLE (11822-7892-7)
- ndc111182278929500 TABLET, COATED in 1 BOTTLE (11822-7892-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A091239
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": "11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d",
"productndc": "11822-7892",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "091239",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Feb 1, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091239",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20200601",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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