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United States · US · US:0573-0151_4cd840a6-9554-de58-e063-6394a90ab543
ADVIL
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHaleon US Holdings LLC
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc1105730151051 BOTTLE in 1 CARTON (0573-0151-05) / 115 TABLET, COATED in 1 BOTTLE
- ndc11057301511010 VIAL in 1 PACKAGE (0573-0151-10) / 10 TABLET, COATED in 1 VIAL
- ndc11057301511210 TABLET, COATED in 1 VIAL (0573-0151-12)
- ndc1105730151133 VIAL in 1 PACKAGE (0573-0151-13) / 10 TABLET, COATED in 1 VIAL
- ndc1105730151202 VIAL in 1 PACKAGE (0573-0151-20) / 10 TABLET, COATED in 1 VIAL
- ndc1105730151211 BOTTLE in 1 CARTON (0573-0151-21) / 36 TABLET, COATED in 1 BOTTLE
- ndc1105730151301 BOTTLE in 1 CARTON (0573-0151-30) / 130 TABLET, COATED in 1 BOTTLE
- ndc1105730151402 BOTTLE in 1 CARTON (0573-0151-40) / 100 TABLET, COATED in 1 BOTTLE
- ndc1105730151482 CARTON in 1 PACKAGE (0573-0151-48) / 1 BOTTLE in 1 CARTON / 100 TABLET, COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
N018989
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": {
"a3c30dd2-75f3-4f8b-88d7-4a63dea5bad7": {
"match": "brand_token",
"title": "ADVIL PM (DIPHENHYDRAMINE CITRATE, IBUPROFEN) TABLET, COATED [NAVAJO MANUFACTURING COMPANY INC.]",
"spl_version": "3",
"published_date": "2026-04-09"
}
},
"productid": "0573-0151_4cd840a6-9554-de58-e063-6394a90ab543",
"productndc": "0573-0151",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "018989",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "May 18, 1984"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "ADVIL",
"active_ingred_unit": "mg/1",
"application_number": "NDA018989",
"marketing_category": "NDA",
"nonproprietary_name": "ibuprofen",
"start_marketing_date": "19840518",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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