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United States · US · US:55910-647_22fb911f-2458-4a41-8c7c-30f9bee8ef73
dg health ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDolgencorp Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1155910647711 BOTTLE in 1 CARTON (55910-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1155910647781 BOTTLE in 1 CARTON (55910-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE
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": {
"5f0514bd-7893-4602-a17b-716fb9947572": {
"match": "brand_token",
"title": "DG HEALTH ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [DOLGENCORP INC]",
"spl_version": "9",
"published_date": "2026-02-10"
}
},
"productid": "55910-647_22fb911f-2458-4a41-8c7c-30f9bee8ef73",
"productndc": "55910-647",
"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": "dg health ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072096",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20210616",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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