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United States · US · US:71335-1396_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 · 10
- ndc11713351396084 TABLET, FILM COATED in 1 BOTTLE (71335-1396-0)
- ndc11713351396120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
- ndc11713351396215 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
- ndc11713351396340 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
- ndc11713351396421 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
- ndc11713351396530 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
- ndc11713351396690 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
- ndc117133513967100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
- ndc117133513968120 TABLET, FILM COATED in 1 BOTTLE (71335-1396-8)
- ndc11713351396960 TABLET, FILM COATED in 1 BOTTLE (71335-1396-9)
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": "71335-1396_840d6421-5e3e-4933-84fb-e5676439b9a0",
"productndc": "71335-1396",
"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": "800"
}Related drugs
Other records sharing ATC code G02CC01.
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