NDC 0135-0607

Panadol Cold and Flu NonDrowsy

Acetaminophen And Phenyleprine Hcl

Panadol Cold and Flu NonDrowsy 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; Phenylephrine Hydrochloride.

Product ID0135-0607_08c94755-c510-4e14-a0df-6672fcbfccf0
NDC0135-0607
Product TypeHuman Otc Drug
Proprietary NamePanadol Cold and Flu NonDrowsy
Generic NameAcetaminophen And Phenyleprine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-06-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength325 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0135-0607-02

3 BLISTER PACK in 1 CARTON (0135-0607-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2017-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0607-01 [00135060701]

Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-01

NDC 0135-0607-03 [00135060703]

Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-01

NDC 0135-0607-02 [00135060702]

Panadol Cold and Flu NonDrowsy TABLET, FILM COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-01

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/1

OpenFDA Data

SPL SET ID:f626ab17-01c9-4493-ba9e-0c8c11146384
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1046378
  • 1923702
  • NDC Crossover Matching brand name "Panadol Cold and Flu NonDrowsy" or generic name "Acetaminophen And Phenyleprine Hcl"

    NDCBrand NameGeneric Name
    0135-0607Panadolacetaminophen and phenyleprine HCl
    0135-7031Panadolacetaminophen and phenyleprine HCl

    Trademark Results [Panadol]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    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.