πΊπΈ
United States Β· US Β· US:72476-365_465138e1-6e59-a9e1-e063-6294a90ae8df
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRETAIL BUSINESS SERVICES,LLC.
CountryUS (United States)
ATC codeG02CC01
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 6
- ndc11724763650550 TABLET in 1 BOTTLE (72476-365-05)
- ndc117247636510100 TABLET in 1 BOTTLE (72476-365-10)
- ndc117247636520200 TABLET in 1 BOTTLE (72476-365-20)
- ndc11724763652424 TABLET in 1 BOTTLE (72476-365-24)
- ndc117247636550500 TABLET in 1 BOTTLE (72476-365-50)
- ndc1172476365991000 TABLET in 1 BOTTLE (72476-365-99)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A079174
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": "72476-365_465138e1-6e59-a9e1-e063-6294a90ae8df",
"productndc": "72476-365",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "079174",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Dec 10, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA079174",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20200726",
"active_numerator_strength": "200"
}Related drugs
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