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United States · US · US:58602-802_5e6a6cce-b25c-4d6c-9d58-b4db175c6f8e
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 · 6
- ndc1158602802071 BOTTLE in 1 CARTON (58602-802-07) / 24 TABLET in 1 BOTTLE
- ndc1158602802141 BOTTLE in 1 CARTON (58602-802-14) / 50 TABLET in 1 BOTTLE
- ndc1158602802211 BOTTLE in 1 CARTON (58602-802-21) / 100 TABLET in 1 BOTTLE
- ndc1158602802291 BOTTLE in 1 CARTON (58602-802-29) / 150 TABLET in 1 BOTTLE
- ndc115860280234200 TABLET in 1 BOTTLE (58602-802-34)
- ndc115860280238300 TABLET in 1 BOTTLE (58602-802-38)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A208865
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": "58602-802_5e6a6cce-b25c-4d6c-9d58-b4db175c6f8e",
"productndc": "58602-802",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "208865",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Nov 8, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208865",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20171108",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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