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United States · US · US:0404-0017_3e4c41a0-acc2-ca87-e063-6294a90a7540
Henry Schein Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHenry Schein Inc.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110404001713250 PACKET in 1 BOX (0404-0017-13) / 2 TABLET, FILM COATED in 1 PACKET (0404-0017-99)
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": {
"267c7c8a-2f3f-1f4d-e054-00144ff8d46c": {
"match": "brand_token",
"title": "HENRY SCHEIN IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [HENRY SCHEIN INC.]",
"spl_version": "12",
"published_date": "2025-09-11"
}
},
"productid": "0404-0017_3e4c41a0-acc2-ca87-e063-6294a90a7540",
"productndc": "0404-0017",
"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": "Henry Schein Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075010",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20151215",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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