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United States · US · US:71335-2689_02d16074-f2b6-4be5-a138-e31fd04f4b9e
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
- ndc11713352689084 TABLET in 1 BOTTLE (71335-2689-0)
- ndc11713352689120 TABLET in 1 BOTTLE (71335-2689-1)
- ndc11713352689215 TABLET in 1 BOTTLE (71335-2689-2)
- ndc11713352689340 TABLET in 1 BOTTLE (71335-2689-3)
- ndc11713352689421 TABLET in 1 BOTTLE (71335-2689-4)
- ndc11713352689530 TABLET in 1 BOTTLE (71335-2689-5)
- ndc11713352689690 TABLET in 1 BOTTLE (71335-2689-6)
- ndc117133526897100 TABLET in 1 BOTTLE (71335-2689-7)
- ndc117133526898120 TABLET in 1 BOTTLE (71335-2689-8)
- ndc11713352689960 TABLET in 1 BOTTLE (71335-2689-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A213794
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": "71335-2689_02d16074-f2b6-4be5-a138-e31fd04f4b9e",
"productndc": "71335-2689",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "213794",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "May 8, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "002",
"approval_date": "May 8, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "003",
"approval_date": "May 8, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA213794",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20200508",
"active_numerator_strength": "800"
}Related drugs
Other records sharing ATC code G02CC01.
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