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United States · US · US:67060-001_feb250d0-cddb-448d-b08d-00a0fc091055
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerADVANCED FIRST AID, INC.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116706000167250 PACKET in 1 CARTON (67060-001-67) / 2 TABLET, FILM COATED in 1 PACKET
- ndc116706000168100 PACKET in 1 CARTON (67060-001-68) / 2 TABLET, FILM COATED in 1 PACKET
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079174
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": "67060-001_feb250d0-cddb-448d-b08d-00a0fc091055",
"productndc": "67060-001",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "079174",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Dec 10, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA079174",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN 200MG",
"start_marketing_date": "20150409",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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