NDC 11673-484

up and up acetaminophen extra strength

Acetaminophen

up and up acetaminophen extra strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Acetaminophen.

Product ID11673-484_5060ccde-cf1e-404c-873f-b71289863eb6
NDC11673-484
Product TypeHuman Otc Drug
Proprietary Nameup and up acetaminophen extra strength
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-02
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameTarget Corporation
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 11673-484-71

1 BOTTLE in 1 CARTON (11673-484-71) > 50 TABLET in 1 BOTTLE
Marketing Start Date2009-12-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-484-71 [11673048471]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-12-02

NDC 11673-484-83 [11673048483]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-03-27

NDC 11673-484-78 [11673048478]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-12-02

NDC 11673-484-62 [11673048462]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-09-19

NDC 11673-484-01 [11673048401]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-02
Marketing End Date2013-10-25

NDC 11673-484-90 [11673048490]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-02

NDC 11673-484-76 [11673048476]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-11-17

NDC 11673-484-52 [11673048452]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-08-26

NDC 11673-484-85 [11673048485]

up and up acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-02

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:dcbf1eaa-f07f-4b46-a6a4-8c5eb5131605
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • NDC Crossover Matching brand name "up and up acetaminophen extra strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    11673-484up and up acetaminophen extra strengthup and up acetaminophen extra strength
    0121-0657AcetaminophenAcetaminophen
    0113-7000Basic Care acetaminophenAcetaminophen
    0113-7484basic care acetaminophenAcetaminophen
    0113-7544Basic Care AcetaminophenAcetaminophen
    0113-7130basic care childrens pain and feverAcetaminophen
    0113-0020good sense childrens pain and feverAcetaminophen
    0113-0212Good Sense Childrens Pain and FeverAcetaminophen
    0113-0608good sense childrens pain and feverAcetaminophen
    0113-0998Good Sense Childrens Pain and FeverAcetaminophen
    0113-0161Good Sense pain and feverAcetaminophen
    0113-0397Good Sense Pain and Feveracetaminophen
    0113-0590Good Sense Pain and Feveracetaminophen
    0113-0946good sense pain and feverAcetaminophen
    0113-8959Good Sense Pain and FeverAcetaminophen
    0113-0025Good Sense Pain ReliefAcetaminophen
    0113-0044Good Sense Pain ReliefAcetaminophen
    0113-0187good sense pain reliefAcetaminophen
    0113-0217good sense pain reliefAcetaminophen
    0113-0227Good Sense Pain ReliefAcetaminophen
    0113-0403good sense pain reliefAcetaminophen
    0113-0484Good Sense Pain ReliefAcetaminophen
    0113-0518good sense pain reliefAcetaminophen
    0113-0544good sense pain reliefAcetaminophen
    0113-1889good sense pain reliefacetaminophen
    0113-1975Good Sense Pain ReliefAcetaminophen
    0031-9301Robitussin Direct Sore Throat Painacetaminophen

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