NDC 0135-0136

PANADOL Extra Strength

Acetaminophen

PANADOL Extra Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Acetaminophen.

Product ID0135-0136_45fc4a8a-26e0-44a5-8033-50dfc8978a13
NDC0135-0136
Product TypeHuman Otc Drug
Proprietary NamePANADOL Extra Strength
Generic NameAcetaminophen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-03-18
Marketing End Date2019-05-31
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN

Packaging

NDC 0135-0136-05

50 PACKET in 1 CARTON (0135-0136-05) > 2 TABLET, FILM COATED in 1 PACKET (0135-0136-09)
Marketing Start Date2011-03-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0136-05 [00135013605]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2019-05-31

NDC 0135-0136-01 [00135013601]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-04-18
Marketing End Date2018-06-30

NDC 0135-0136-04 [00135013604]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2018-12-31

NDC 0135-0136-03 [00135013603]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2019-04-30

NDC 0135-0136-09 [00135013609]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-10
Marketing End Date2019-05-31

NDC 0135-0136-02 [00135013602]

PANADOL Extra Strength TABLET, FILM COATED
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-18
Marketing End Date2019-04-30

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:62920a3f-c662-4db2-a4aa-8170a23ed3b6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • 200977

    • NDC Crossover Matching brand name "PANADOL Extra Strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    0135-0136PANADOL Extra StrengthPANADOL Extra Strength
    0135-0609PANADOL Extra StrengthPANADOL 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

    Trademark Results [PANADOL]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PANADOL
    PANADOL
    98688417 not registered Live/Pending
    Haleon UK IP Limited
    2024-08-08
    PANADOL
    PANADOL
    98675464 not registered Live/Pending
    Haleon UK IP Limited
    2024-07-31
    PANADOL
    PANADOL
    87707023 5512890 Live/Registered
    GlaxoSmithKline Consumer Healthcare (UK) IP Limited
    2017-12-04
    PANADOL
    PANADOL
    85678959 4408281 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (UK) IP LIMITED
    2012-07-17
    PANADOL
    PANADOL
    73094226 1060597 Live/Registered
    STERLING DRUG INC.
    1976-07-22
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.