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United States · US · US:0135-7011_10c12d49-cd3c-e104-e063-6294a90a4e5a
PANADOL
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 · 4
- ndc1101357011012 TABLET, FILM COATED in 1 POUCH (0135-7011-01)
- ndc1101357011021 BOTTLE in 1 CARTON (0135-7011-02) / 24 TABLET, FILM COATED in 1 BOTTLE
- ndc1101357011031 BOTTLE in 1 CARTON (0135-7011-03) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1101357011041 BOTTLE in 1 CARTON (0135-7011-04) / 100 TABLET, FILM COATED 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": {
"341761b9-f0be-f816-e063-6394a90a5e63": {
"match": "brand_token",
"title": "PANADOL COLD AND FLU DAY (ACETAMINOPHEN, DEXTROMETHORPHAN HBR) TABLET [HALEON US HOLDINGS LLC]",
"spl_version": "2",
"published_date": "2026-04-30"
}
},
"productid": "0135-7011_10c12d49-cd3c-e104-e063-6294a90a4e5a",
"productndc": "0135-7011",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "PANADOL",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "acetaminophen",
"start_marketing_date": "20210215",
"active_numerator_strength": "500"
}Related drugs
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