NDC 69842-484

acetaminophen

Acetaminophen

acetaminophen is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Cvs Pharmacy. The primary component is Acetaminophen.

Product ID69842-484_88eb31c8-05f9-4659-963f-eff66f9612ff
NDC69842-484
Product TypeHuman Otc Drug
Proprietary Nameacetaminophen
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-06-12
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameCVS Pharmacy
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 69842-484-47

1 BOTTLE in 1 CARTON (69842-484-47) > 150 TABLET in 1 BOTTLE
Marketing Start Date2018-06-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69842-484-93 [69842048493]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-06-12

NDC 69842-484-78 [69842048478]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-06-12

NDC 69842-484-47 [69842048447]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-06-12

NDC 69842-484-90 [69842048490]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-06-12

NDC 69842-484-71 [69842048471]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-06-12

NDC 69842-484-62 [69842048462]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-06-12

NDC 69842-484-83 [69842048483]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-06-12

NDC 69842-484-87 [69842048487]

acetaminophen TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-06-12

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:fc2d4367-8884-4b76-aa3e-8c35be1ace49
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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.