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United States · US · US:68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4
Acetaminophen
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11680715239330 TABLET in 1 BOTTLE (68071-5239-3)
- ndc11680715239545 TABLET in 1 BOTTLE (68071-5239-5)
- ndc11680715239990 TABLET in 1 BOTTLE (68071-5239-9)
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": "68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4",
"productndc": "68071-5239",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Acetaminophen",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Extra Strength Pain Relief",
"start_marketing_date": "19890101",
"active_numerator_strength": "500"
}Related drugs
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