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United States · US · US:58602-843_4a614548-3e17-4ead-97d2-634996a5b490
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurohealth LLC
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 13
- ndc1158602843121 BOTTLE in 1 CARTON (58602-843-12) / 40 CAPSULE in 1 BOTTLE
- ndc1158602843181 BOTTLE in 1 CARTON (58602-843-18) / 80 CAPSULE in 1 BOTTLE
- ndc115860284330160 CAPSULE in 1 BOTTLE (58602-843-30)
- ndc115860284332180 CAPSULE in 1 BOTTLE (58602-843-32)
- ndc115860284334200 CAPSULE in 1 BOTTLE, PLASTIC (58602-843-34)
- ndc115860284338300 CAPSULE in 1 BOTTLE (58602-843-38)
- ndc1158602843701 BOTTLE, PLASTIC in 1 CARTON (58602-843-70) / 40 CAPSULE in 1 BOTTLE, PLASTIC
- ndc1158602843721 BOTTLE, PLASTIC in 1 CARTON (58602-843-72) / 80 CAPSULE in 1 BOTTLE, PLASTIC
- ndc1158602843731 BOTTLE in 1 CARTON (58602-843-73) / 20 CAPSULE in 1 BOTTLE
- ndc115860284374160 CAPSULE in 1 BOTTLE, PLASTIC (58602-843-74)
- ndc115860284375300 CAPSULE in 1 BOTTLE, PLASTIC (58602-843-75)
- ndc1158602843792 BOTTLE in 1 CARTON (58602-843-79) / 180 CAPSULE in 1 BOTTLE
- ndc115860284392180 CAPSULE in 1 BOTTLE, PLASTIC (58602-843-92)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A207753
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": "58602-843_4a614548-3e17-4ead-97d2-634996a5b490",
"productndc": "58602-843",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "207753",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
"product_no": "001",
"approval_date": "Jun 29, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA207753",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20200715",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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