🇺🇸
United States · US · US:71335-1503_840d6421-5e3e-4933-84fb-e5676439b9a0
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
- ndc11713351503021 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)
- ndc11713351503120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)
- ndc11713351503215 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)
- ndc11713351503330 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)
- ndc11713351503440 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)
- ndc11713351503560 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)
- ndc11713351503690 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)
- ndc117133515037120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)
- ndc11713351503850 TABLET, FILM COATED in 1 BOTTLE (71335-1503-8)
- ndc117133515039100 TABLET, FILM COATED in 1 BOTTLE (71335-1503-9)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A090796
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": "71335-1503_840d6421-5e3e-4933-84fb-e5676439b9a0",
"productndc": "71335-1503",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "090796",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Dec 21, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "600MG",
"product_no": "002",
"approval_date": "Dec 21, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "003",
"approval_date": "Dec 21, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090796",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20151230",
"active_numerator_strength": "600"
}Related drugs
Other records sharing ATC code G02CC01.
Access this data programmatically
Query IBUPROFEN and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.