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United States · US · US:83209-464_1a0301ba-9f66-ac39-e063-6394a90a34bb
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoswell Pharmacy Services LLC d/b/a BPS Wholesale
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 13
- ndc1183209464099 TABLET in 1 BLISTER PACK (83209-464-09)
- ndc11832094641010 TABLET in 1 BLISTER PACK (83209-464-10)
- ndc11832094641212 TABLET in 1 BLISTER PACK (83209-464-12)
- ndc11832094641414 TABLET in 1 BLISTER PACK (83209-464-14)
- ndc11832094641515 TABLET in 1 BLISTER PACK (83209-464-15)
- ndc11832094641818 TABLET in 1 BLISTER PACK (83209-464-18)
- ndc11832094642020 TABLET in 1 BLISTER PACK (83209-464-20)
- ndc11832094642121 TABLET in 1 BLISTER PACK (83209-464-21)
- ndc11832094642424 TABLET in 1 BLISTER PACK (83209-464-24)
- ndc11832094642828 TABLET in 1 BLISTER PACK (83209-464-28)
- ndc11832094643030 TABLET in 1 BLISTER PACK (83209-464-30)
- ndc11832094644040 TABLET in 1 BLISTER PACK (83209-464-40)
- ndc11832094646060 TABLET in 1 BLISTER PACK (83209-464-60)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A078558
ABABAB
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": "83209-464_1a0301ba-9f66-ac39-e063-6394a90a34bb",
"productndc": "83209-464",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "078558",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Jun 18, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "002",
"approval_date": "Jun 18, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "003",
"approval_date": "Jun 18, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078558",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20240603",
"active_numerator_strength": "400"
}Related drugs
Other records sharing ATC code G02CC01.
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