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United States · US · US:71335-1911_97810365-78c2-4332-87e7-c873715fea15
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
- ndc11713351911090 TABLET, FILM COATED in 1 BOTTLE (71335-1911-0)
- ndc11713351911120 TABLET, FILM COATED in 1 BOTTLE (71335-1911-1)
- ndc11713351911215 TABLET, FILM COATED in 1 BOTTLE (71335-1911-2)
- ndc11713351911330 TABLET, FILM COATED in 1 BOTTLE (71335-1911-3)
- ndc117133519114100 TABLET, FILM COATED in 1 BOTTLE (71335-1911-4)
- ndc11713351911560 TABLET, FILM COATED in 1 BOTTLE (71335-1911-5)
- ndc11713351911650 TABLET, FILM COATED in 1 BOTTLE (71335-1911-6)
- ndc11713351911740 TABLET, FILM COATED in 1 BOTTLE (71335-1911-7)
- ndc11713351911810 TABLET, FILM COATED in 1 BOTTLE (71335-1911-8)
- ndc11713351911956 TABLET, FILM COATED in 1 BOTTLE (71335-1911-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A072096
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": "71335-1911_97810365-78c2-4332-87e7-c873715fea15",
"productndc": "71335-1911",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "072096",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Dec 8, 1987"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072096",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20180920",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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