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United States · US · US:55910-518_36204b38-c646-3f83-e063-6294a90a6977
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDOLGENCORP INC
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1155910518111 BOTTLE in 1 CARTON (55910-518-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1155910518151 BOTTLE in 1 CARTON (55910-518-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc115591051822120 CAPSULE, LIQUID FILLED in 1 BOTTLE (55910-518-22)
- ndc115591051826200 CAPSULE, LIQUID FILLED in 1 BOTTLE (55910-518-26)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A078682
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": "55910-518_36204b38-c646-3f83-e063-6294a90a6977",
"productndc": "55910-518",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "078682",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
"product_no": "001",
"approval_date": "Mar 24, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078682",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20231026",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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