NDC 55312-484

acetaminophen extra strength

Acetaminophen

acetaminophen extra strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Western Family Foods Inc. The primary component is Acetaminophen.

Product ID55312-484_1f7ad2c3-120a-43fc-bf96-beba166d4ff2
NDC55312-484
Product TypeHuman Otc Drug
Proprietary Nameacetaminophen extra strength
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-03-14
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameWestern Family Foods Inc
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 55312-484-90

500 TABLET in 1 BOTTLE (55312-484-90)
Marketing Start Date2008-03-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55312-484-52 [55312048452]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-90 [55312048490]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-78 [55312048478]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-02 [55312048402]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-82 [55312048482]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-62 [55312048462]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

NDC 55312-484-71 [55312048471]

acetaminophen extra strength TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-03-14

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:09a2bf1e-8518-4dca-87a0-bf41e5fcedb2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • NDC Crossover Matching brand name "acetaminophen extra strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    68196-919acetaminophen extra strengthacetaminophen extra strength
    69842-931Acetaminophen Extra StrengthAcetaminophen Extra Strength
    69842-531Acetaminophen Extra StrengthAcetaminophen Extra Strength
    69842-750Acetaminophen Extra StrengthAcetaminophen Extra Strength
    69842-945Acetaminophen Extra StrengthAcetaminophen Extra Strength
    70000-0312Acetaminophen Extra StrengthAcetaminophen Extra Strength
    71141-115Acetaminophen Extra StrengthAcetaminophen Extra Strength
    11673-519acetaminophen Extra Strengthacetaminophen Extra Strength
    33992-0175Acetaminophen Extra StrengthAcetaminophen Extra Strength
    33992-0016Acetaminophen Extra StrengthAcetaminophen Extra Strength
    37012-770Acetaminophen Extra StrengthAcetaminophen Extra Strength
    41163-500Acetaminophen Extra StrengthAcetaminophen Extra Strength
    41520-919Acetaminophen Extra StrengthAcetaminophen Extra Strength
    46994-175Acetaminophen Extra StrengthAcetaminophen Extra Strength
    46994-935Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49035-158Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49035-531Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49035-457Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49035-519Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49035-175Acetaminophen Extra StrengthAcetaminophen Extra Strength
    49483-341ACETAMINOPHEN EXTRA STRENGTHACETAMINOPHEN EXTRA STRENGTH
    51824-011Acetaminophen Extra StrengthAcetaminophen Extra Strength
    51824-012Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55301-519Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55319-059Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55312-484acetaminophen extra strengthacetaminophen extra strength
    55319-531Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55319-457Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55319-541Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55319-519Acetaminophen Extra StrengthAcetaminophen Extra Strength
    55319-041Acetaminophen Extra StrengthAcetaminophen Extra Strength
    67091-133Acetaminophen Extra StrengthAcetaminophen 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

    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.