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United States · US · US:58602-902_f2654aa5-8bb3-4f27-9495-0d31c18bf5f8
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 · 11
- ndc1158602902121 BOTTLE in 1 CARTON (58602-902-12) / 40 CAPSULE in 1 BOTTLE
- ndc1158602902181 BOTTLE in 1 CARTON (58602-902-18) / 80 CAPSULE in 1 BOTTLE
- ndc115860290230160 CAPSULE in 1 BOTTLE (58602-902-30)
- ndc115860290232180 CAPSULE in 1 BOTTLE, PLASTIC (58602-902-32)
- ndc115860290234200 CAPSULE in 1 BOTTLE, PLASTIC (58602-902-34)
- ndc115860290238300 CAPSULE in 1 BOTTLE (58602-902-38)
- ndc1158602902701 BOTTLE, PLASTIC in 1 CARTON (58602-902-70) / 40 CAPSULE in 1 BOTTLE, PLASTIC
- ndc1158602902721 BOTTLE, PLASTIC in 1 CARTON (58602-902-72) / 80 CAPSULE in 1 BOTTLE, PLASTIC
- ndc1158602902731 BOTTLE in 1 CARTON (58602-902-73) / 20 CAPSULE in 1 BOTTLE
- ndc115860290274160 CAPSULE in 1 BOTTLE, PLASTIC (58602-902-74)
- ndc115860290275300 CAPSULE in 1 BOTTLE, PLASTIC (58602-902-75)
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": "58602-902_f2654aa5-8bb3-4f27-9495-0d31c18bf5f8",
"productndc": "58602-902",
"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": "20180629",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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