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United States · US · US:0363-9612_13b22280-b329-93b4-e063-6394a90a12f9
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREENS
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc110363961201100 TABLET in 1 BOTTLE, PLASTIC (0363-9612-01)
- ndc11036396120550 TABLET in 1 BOTTLE, PLASTIC (0363-9612-05)
- ndc110363961226225 TABLET in 1 BOTTLE, PLASTIC (0363-9612-26)
- ndc110363961250500 TABLET in 1 BOTTLE, PLASTIC (0363-9612-50)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A091237
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": "0363-9612_13b22280-b329-93b4-e063-6394a90a12f9",
"productndc": "0363-9612",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "091237",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Feb 8, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091237",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20181211",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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