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United States · US · US:69168-335_efd20a4b-fd12-46e4-ad80-5065264a4203
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllegiant Health
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc116916833501100 TABLET in 1 BOX (69168-335-01)
- ndc116916833503250 TABLET in 1 BOTTLE (69168-335-03)
- ndc11691683353030 TABLET in 1 BOX (69168-335-30)
- ndc11691683354040 TABLET in 1 BOX (69168-335-40)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079129
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": "69168-335_efd20a4b-fd12-46e4-ad80-5065264a4203",
"productndc": "69168-335",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "079129",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 28, 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": "ANDA079129",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen 200 mg",
"start_marketing_date": "20141219",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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