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United States · US · US:0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca
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
- ndc1101350609011 BOTTLE in 1 CARTON (0135-0609-01) / 24 TABLET, FILM COATED in 1 BOTTLE
- ndc1101350609021 BOTTLE in 1 CARTON (0135-0609-02) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1101350609031 BOTTLE in 1 CARTON (0135-0609-03) / 100 TABLET, FILM COATED in 1 BOTTLE
- ndc11013506090450 PACKET in 1 CARTON (0135-0609-04) / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)
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": "0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca",
"productndc": "0135-0609",
"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": "20170315",
"active_numerator_strength": "500"
}Related drugs
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