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United States · US · US:63629-1467_8445f638-124d-40e8-82ea-39dfa70f8a6b
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
- ndc11636291467090 TABLET, FILM COATED in 1 BOTTLE (63629-1467-0)
- ndc11636291467120 TABLET, FILM COATED in 1 BOTTLE (63629-1467-1)
- ndc11636291467215 TABLET, FILM COATED in 1 BOTTLE (63629-1467-2)
- ndc11636291467330 TABLET, FILM COATED in 1 BOTTLE (63629-1467-3)
- ndc116362914674100 TABLET, FILM COATED in 1 BOTTLE (63629-1467-4)
- ndc11636291467560 TABLET, FILM COATED in 1 BOTTLE (63629-1467-5)
- ndc11636291467650 TABLET, FILM COATED in 1 BOTTLE (63629-1467-6)
- ndc11636291467740 TABLET, FILM COATED in 1 BOTTLE (63629-1467-7)
- ndc11636291467810 TABLET, FILM COATED in 1 BOTTLE (63629-1467-8)
- ndc11636291467956 TABLET, FILM COATED in 1 BOTTLE (63629-1467-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075010
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": "63629-1467_8445f638-124d-40e8-82ea-39dfa70f8a6b",
"productndc": "63629-1467",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075010",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 1, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075010",
"marketing_category": "ANDA",
"nonproprietary_name": "ibuprofen",
"start_marketing_date": "20040101",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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