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United States · US · US:71335-1517_840d6421-5e3e-4933-84fb-e5676439b9a0
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc11713351517120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)
- ndc11713351517230 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2)
- ndc11713351517340 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3)
- ndc11713351517460 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4)
- ndc11713351517590 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5)
- ndc117133515176120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6)
- ndc117133515177100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7)
- ndc11713351517821 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8)
- ndc11713351517915 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A090796
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": "71335-1517_840d6421-5e3e-4933-84fb-e5676439b9a0",
"productndc": "71335-1517",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "090796",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Dec 21, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "002",
"approval_date": "Dec 21, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "003",
"approval_date": "Dec 21, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090796",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20151230",
"active_numerator_strength": "400"
}Related drugs
Other records sharing ATC code G02CC01.
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