🇺🇸
United States · US · US:0067-2200_4b6b07e6-a9df-37df-e063-6394a90a3157
Excedrin
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHaleon US Holdings LLC
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1100672200201 BOTTLE in 1 CARTON (0067-2200-20) / 20 TABLET in 1 BOTTLE
- ndc1100672200801 BOTTLE in 1 CARTON (0067-2200-80) / 80 TABLET in 1 BOTTLE
- ndc1100672200821 BOTTLE in 1 CARTON (0067-2200-82) / 160 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "362O9ITL9D",
"rxcui": "161",
"inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
"display_name": "ACETAMINOPHEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4efbd21b-92fe-96a7-e063-6294a90ac4ad": {
"match": "brand_token",
"title": "EXCEDRIN MIGRAINE (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]",
"spl_version": "1",
"published_date": "2026-04-10"
}
},
"productid": "0067-2200_4b6b07e6-a9df-37df-e063-6394a90a3157",
"productndc": "0067-2200",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Excedrin",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "acetaminophen",
"start_marketing_date": "20260331",
"active_numerator_strength": "500"
}Related drugs
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