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United States · US · US:71335-2682_e1aa3e81-8aa9-445a-921d-f7f3d2712fd6
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
- ndc11713352682120 TABLET in 1 BOTTLE (71335-2682-1)
- ndc11713352682230 TABLET in 1 BOTTLE (71335-2682-2)
- ndc11713352682340 TABLET in 1 BOTTLE (71335-2682-3)
- ndc11713352682460 TABLET in 1 BOTTLE (71335-2682-4)
- ndc11713352682590 TABLET in 1 BOTTLE (71335-2682-5)
- ndc117133526826120 TABLET in 1 BOTTLE (71335-2682-6)
- ndc117133526827100 TABLET in 1 BOTTLE (71335-2682-7)
- ndc11713352682821 TABLET in 1 BOTTLE (71335-2682-8)
- ndc11713352682915 TABLET in 1 BOTTLE (71335-2682-9)
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": "71335-2682_e1aa3e81-8aa9-445a-921d-f7f3d2712fd6",
"productndc": "71335-2682",
"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": "400"
}Related drugs
Other records sharing ATC code G02CC01.
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