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United States · US · US:0363-4381_84215331-f3fd-489b-a67f-9eebd1fe1322
Dye Free Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWalgreen Company
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1103634381121 BOTTLE, PLASTIC in 1 CARTON (0363-4381-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075139
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": {
"46846abe-062d-a11f-e063-6294a90a73f3": {
"match": "brand_token",
"title": "DYE FREE REGULAR STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) SUSPENSION [WALMART INC.]",
"spl_version": "2",
"published_date": "2026-02-26"
}
},
"productid": "0363-4381_84215331-f3fd-489b-a67f-9eebd1fe1322",
"productndc": "0363-4381",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075139",
"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": "Dye Free Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075139",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "19990301",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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