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United States · US · US:0363-1610_13af6333-7380-e54c-e063-6294a90aaa35
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 · 5
- ndc11036316102320 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-23)
- ndc110363161031300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-31)
- ndc11036316104440 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-44)
- ndc110363161066160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-66)
- ndc11036316108080 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-80)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079205
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": "0363-1610_13af6333-7380-e54c-e063-6294a90aaa35",
"productndc": "0363-1610",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "079205",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
"product_no": "001",
"approval_date": "Jun 26, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA079205",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20160127",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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