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United States · US · US:0573-0230_5b08a4cf-a90b-42ed-b449-c250cdc0a5f4
Advil Menstrual Pain
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 · 2
- ndc1105730230201 BOTTLE in 1 CARTON (0573-0230-20) / 20 TABLET, COATED in 1 BOTTLE
- ndc1105730230401 BOTTLE in 1 CARTON (0573-0230-40) / 40 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": "0573-0230_5b08a4cf-a90b-42ed-b449-c250cdc0a5f4",
"productndc": "0573-0230",
"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 Menstrual Pain",
"active_ingred_unit": "mg/1",
"application_number": "NDA201803",
"marketing_category": "NDA",
"nonproprietary_name": "ibuprofen sodium",
"start_marketing_date": "20160630",
"active_numerator_strength": "256"
}Related drugs
Other records sharing ATC code G02CC01.
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