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United States · US · US:66267-115_1bbdab14-0ce5-b300-e063-6394a90a5175
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11662671152020 TABLET, FILM COATED in 1 BOTTLE (66267-115-20)
- ndc11662671153030 TABLET, FILM COATED in 1 BOTTLE (66267-115-30)
- ndc11662671155050 TABLET, FILM COATED in 1 BOTTLE (66267-115-50)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075010
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": "66267-115_1bbdab14-0ce5-b300-e063-6394a90a5175",
"productndc": "66267-115",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075010",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 1, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075010",
"marketing_category": "ANDA",
"nonproprietary_name": "ibuprofen",
"start_marketing_date": "20040101",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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