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United States · US · US:71205-357_c18cb763-af0c-4cc2-b7df-520835c91884
ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc1171205357066 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)
- ndc11712053572424 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)
- ndc11712053573030 TABLET, FILM COATED in 1 BOTTLE (71205-357-30)
- ndc11712053575050 TABLET, FILM COATED in 1 BOTTLE (71205-357-50)
- ndc11712053576060 TABLET, FILM COATED in 1 BOTTLE (71205-357-60)
- ndc11712053579090 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)
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": "71205-357_c18cb763-af0c-4cc2-b7df-520835c91884",
"productndc": "71205-357",
"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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