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United States · US · US:63629-1470_fa931f19-3b64-492e-9bd6-0be85e037dc9
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
- ndc11636291470084 TABLET in 1 BOTTLE (63629-1470-0)
- ndc11636291470120 TABLET in 1 BOTTLE (63629-1470-1)
- ndc11636291470242 TABLET in 1 BOTTLE (63629-1470-2)
- ndc11636291470340 TABLET in 1 BOTTLE (63629-1470-3)
- ndc11636291470421 TABLET in 1 BOTTLE (63629-1470-4)
- ndc11636291470530 TABLET in 1 BOTTLE (63629-1470-5)
- ndc11636291470690 TABLET in 1 BOTTLE (63629-1470-6)
- ndc116362914707100 TABLET in 1 BOTTLE (63629-1470-7)
- ndc116362914708120 TABLET in 1 BOTTLE (63629-1470-8)
- ndc11636291470960 TABLET in 1 BOTTLE (63629-1470-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A078558
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": "63629-1470_fa931f19-3b64-492e-9bd6-0be85e037dc9",
"productndc": "63629-1470",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "078558",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Jun 18, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "002",
"approval_date": "Jun 18, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "003",
"approval_date": "Jun 18, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078558",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20091123",
"active_numerator_strength": "800"
}Related drugs
Other records sharing ATC code G02CC01.
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