NDC 52959-002

ACETAMINOPHEN

Acetaminophen

ACETAMINOPHEN is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Acetaminophen.

Product ID52959-002_75266931-335f-fc14-e053-2991aa0a84ed
NDC52959-002
Product TypeHuman Otc Drug
Proprietary NameACETAMINOPHEN
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2001-10-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameH.J. Harkins Company, Inc.
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 52959-002-50

50 TABLET in 1 BOTTLE (52959-002-50)
Marketing Start Date2001-10-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52959-002-14 [52959000214]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-50 [52959000250]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-15 [52959000215]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-20 [52959000220]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-10 [52959000210]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-40 [52959000240]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-42 [52959000242]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-90 [52959000290]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-45 [52959000245]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-25 [52959000225]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-30 [52959000230]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

NDC 52959-002-24 [52959000224]

ACETAMINOPHEN TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2001-10-08
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:75266931-335e-fc14-e053-2991aa0a84ed
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440

    • NDC Crossover Matching brand name "ACETAMINOPHEN" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    0121-0657AcetaminophenAcetaminophen
    68016-656AcetaminophenAcetaminophen
    68016-657AcetaminophenAcetaminophen
    68016-655AcetaminophenAcetaminophen
    68210-0022ACETAMINOPHENACETAMINOPHEN
    68210-0023ACETAMINOPHENACETAMINOPHEN
    68387-214ACETAMINOPHENACETAMINOPHEN
    0536-1172AcetaminophenAcetaminophen
    0536-3233AcetaminophenAcetaminophen
    69477-000AcetaminophenAcetaminophen
    69517-628AcetaminophenAcetaminophen
    69517-623AcetaminophenAcetaminophen
    69517-627AcetaminophenAcetaminophen
    69584-012AcetaminophenAcetaminophen
    69517-624AcetaminophenAcetaminophen
    69842-298AcetaminophenAcetaminophen
    69842-168acetaminophenacetaminophen
    69842-311AcetaminophenAcetaminophen
    69842-465AcetaminophenAcetaminophen
    69842-484acetaminophenacetaminophen
    69842-707acetaminophenacetaminophen
    69842-930AcetaminophenAcetaminophen
    70000-0153ACETAMINOPHENACETAMINOPHEN
    70000-0104AcetaminophenAcetaminophen
    70000-0152AcetaminophenAcetaminophen
    70000-0410AcetaminophenAcetaminophen
    70000-0151AcetaminophenAcetaminophen
    70000-0446AcetaminophenAcetaminophen
    70000-0150ACETAMINOPHENACETAMINOPHEN
    70518-1101ACETAMINOPHENACETAMINOPHEN
    70518-1915AcetaminophenAcetaminophen
    70518-1930AcetaminophenAcetaminophen
    70518-1840AcetaminophenAcetaminophen
    71141-004AcetaminophenAcetaminophen
    0615-0591AcetaminophenAcetaminophen
    71247-129AcetaminophenAcetaminophen
    71205-165AcetaminophenAcetaminophen
    0615-2542AcetaminophenAcetaminophen
    71321-100AcetaminophenAcetaminophen
    0615-4510AcetaminophenAcetaminophen
    0615-4554AcetaminophenAcetaminophen
    71610-238AcetaminophenAcetaminophen
    76168-010AcetaminophenAcetaminophen
    72570-100AcetaminophenAcetaminophen
    76168-120AcetaminophenAcetaminophen
    76413-301AcetaminophenAcetaminophen
    0615-8250AcetaminophenAcetaminophen
    0904-6749AcetaminophenAcetaminophen
    0904-6719AcetaminophenAcetaminophen
    0904-6720acetaminophenacetaminophen

    Trademark Results [ACETAMINOPHEN]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACETAMINOPHEN
    ACETAMINOPHEN
    85615223 not registered Dead/Abandoned
    General Merchandise importers and Expoters
    2012-05-03
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