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United States · US · US:72476-112_43e1851f-a126-8f4d-e063-6294a90a04e9
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRETAIL BUSINESS SERVICES , LLC.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1172476112021 BOTTLE, PLASTIC in 1 CARTON (72476-112-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
- ndc1172476112031 BOTTLE, PLASTIC in 1 CARTON (72476-112-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A202312
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": "72476-112_43e1851f-a126-8f4d-e063-6294a90a04e9",
"productndc": "72476-112",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "202312",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Oct 7, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202312",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20200201",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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