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United States · US · US:0573-0133_40429ef4-846a-eb4c-e063-6394a90ab7a9
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 · 12
- ndc1105730133013000 PACKET in 1 CASE (0573-0133-01) / 2 TABLET, COATED in 1 PACKET
- ndc11057301330250 PACKET in 1 TRAY (0573-0133-02) / 2 TABLET, COATED in 1 PACKET
- ndc1105730133042 PACKET in 1 BLISTER PACK (0573-0133-04) / 2 TABLET, COATED in 1 PACKET
- ndc1105730133052 PACKET in 1 CARTON (0573-0133-05) / 2 TABLET, COATED in 1 PACKET
- ndc1105730133201 BOTTLE in 1 CARTON (0573-0133-20) / 20 TABLET, COATED in 1 BOTTLE
- ndc1105730133401 BOTTLE in 1 CARTON (0573-0133-40) / 40 TABLET, COATED in 1 BOTTLE
- ndc1105730133411 BOTTLE in 1 CARTON (0573-0133-41) / 40 TABLET, COATED in 1 BOTTLE
- ndc1105730133801 BOTTLE in 1 CARTON (0573-0133-80) / 80 TABLET, COATED in 1 BOTTLE
- ndc1105730133811 BOTTLE in 1 CARTON (0573-0133-81) / 100 TABLET, COATED in 1 BOTTLE
- ndc1105730133882 BOTTLE in 1 PACKAGE (0573-0133-88) / 120 TABLET, COATED in 1 BOTTLE
- ndc1105730133891 BOTTLE in 1 CARTON (0573-0133-89) / 160 TABLET, COATED in 1 BOTTLE
- ndc1105730133911 BOTTLE in 1 CARTON (0573-0133-91) / 180 TABLET, COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
RM1CE97Z4N
IBUPROFEN SODIUM
Orange Book
N201803
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "RM1CE97Z4N",
"rxcui": null,
"inchikey": "VTGPMVCGAVZLQI-UHFFFAOYSA-M",
"display_name": "IBUPROFEN SODIUM",
"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": "0573-0133_40429ef4-846a-eb4c-e063-6394a90ab7a9",
"productndc": "0573-0133",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "201803",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Jun 12, 2012"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN SODIUM",
"proprietary_name": "Advil",
"active_ingred_unit": "mg/1",
"application_number": "NDA201803",
"marketing_category": "NDA",
"nonproprietary_name": "ibuprofen sodium",
"start_marketing_date": "20130708",
"active_numerator_strength": "256"
}Related drugs
Other records sharing ATC code G02CC01.
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