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United States · US · US:42507-647_540e3bdd-bc24-4016-a8e3-ef9d0af384ea
ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHyVee Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1142507647621 BOTTLE in 1 CARTON (42507-647-62) / 24 TABLET, FILM COATED in 1 BOTTLE
- ndc1142507647711 BOTTLE in 1 CARTON (42507-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE (42507-647-50)
- ndc1142507647781 BOTTLE in 1 CARTON (42507-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE (42507-647-00)
- ndc114250764790500 TABLET, FILM COATED in 1 BOTTLE (42507-647-90)
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": "42507-647_540e3bdd-bc24-4016-a8e3-ef9d0af384ea",
"productndc": "42507-647",
"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": "19890715",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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