NDC 59779-544

arthritis pain relief temporary minor

Acetaminophen

arthritis pain relief temporary minor is a Oral Tablet, Film Coated, Extended Release in the Human Otc Drug category. It is labeled and distributed by Cvs Pharmacy. The primary component is Acetaminophen.

Product ID59779-544_cd263063-cac9-4999-afb8-6928cdde3d78
NDC59779-544
Product TypeHuman Otc Drug
Proprietary Namearthritis pain relief temporary minor
Generic NameAcetaminophen
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2000-05-31
Marketing End Date2019-12-31
Marketing CategoryANDA / ANDA
Application NumberANDA075077
Labeler NameCVS Pharmacy
Substance NameACETAMINOPHEN
Active Ingredient Strength650 mg/1
NDC Exclude FlagN

Packaging

NDC 59779-544-47

1 BOTTLE in 1 CARTON (59779-544-47) > 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Marketing Start Date2006-04-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59779-544-71 [59779054471]

arthritis pain relief temporary minor TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075077
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-08-27
Marketing End Date2019-12-31

NDC 59779-544-62 [59779054462]

arthritis pain relief temporary minor TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075077
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-08-27
Marketing End Date2019-10-31

NDC 59779-544-78 [59779054478]

arthritis pain relief temporary minor TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075077
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2000-05-31
Marketing End Date2019-08-31

NDC 59779-544-47 [59779054447]

arthritis pain relief temporary minor TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075077
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2006-04-20
Marketing End Date2019-05-15

NDC 59779-544-85 [59779054485]

arthritis pain relief temporary minor TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075077
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-04-20
Marketing End Date2019-07-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN650 mg/1

OpenFDA Data

SPL SET ID:1526cd5e-8039-4a7e-94e8-b77d901b6d0f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1148399
  • NDC Crossover Matching brand name "arthritis pain relief temporary minor" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    30142-544arthritis pain relief temporary minorarthritis pain relief temporary minor
    59779-544arthritis pain relief temporary minorarthritis pain relief temporary minor
    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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