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United States · US · US:71399-1025_4f2159a1-3ea8-1684-e063-6294a90a8fda
ACETAMINOPHEN
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAkron Pharma Inc.
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc117139910251100 TABLET in 1 BOTTLE (71399-1025-1)
- ndc1171399102521000 TABLET in 1 BOTTLE (71399-1025-2)
- ndc117139910253100 POUCH in 1 PACKAGE (71399-1025-3) / 1 TABLET in 1 POUCH
- ndc11713991025650 TABLET in 1 BOTTLE (71399-1025-6)
- ndc117139910258100000 TABLET in 1 DRUM (71399-1025-8)
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": {
"44520aa1-b63f-4239-e063-6394a90a5e14": {
"match": "brand_token",
"title": "ACETAMINOPHEN LIQUID / ACETAMINOPHEN DIPHENHYDRAMINE HCL LIQUID (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) KIT [KROGER]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "71399-1025_4f2159a1-3ea8-1684-e063-6294a90a8fda",
"productndc": "71399-1025",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "ACETAMINOPHEN",
"active_ingred_unit": "mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen",
"start_marketing_date": "20241206",
"active_numerator_strength": "325"
}Related drugs
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