NDC 0067-2070

NoDoz MAXIMUM STRENGTH ALERTNESS AID

Caffeine

NoDoz MAXIMUM STRENGTH ALERTNESS AID is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Caffeine.

Product ID0067-2070_89a9d8ce-facb-4476-b2df-3717973a1b10
NDC0067-2070
Product TypeHuman Otc Drug
Proprietary NameNoDoz MAXIMUM STRENGTH ALERTNESS AID
Generic NameCaffeine
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2009-12-31
Marketing End Date2019-07-11
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart340
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameCAFFEINE
Active Ingredient Strength200 mg/1
NDC Exclude FlagN

Packaging

NDC 0067-2070-60

1 BOTTLE in 1 CARTON (0067-2070-60) > 60 TABLET, COATED in 1 BOTTLE
Marketing Start Date2009-12-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0067-2070-10 [00067207010]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart340
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-12-31
Marketing End Date2014-12-31

NDC 0067-2070-36 [00067207036]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart340
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-12-31
Marketing End Date2014-12-31

NDC 0067-2070-16 [00067207016]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart340
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-12-31
Marketing End Date2014-12-31

NDC 0067-2070-60 [00067207060]

NoDoz MAXIMUM STRENGTH ALERTNESS AID TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart340
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-12-31
Marketing End Date2019-07-11

Drug Details

Active Ingredients

IngredientStrength
CAFFEINE200 mg/1

OpenFDA Data

SPL SET ID:7ef8b03c-245a-424f-bf75-438559c4418b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198520
  • 795925
  • NDC Crossover Matching brand name "NoDoz MAXIMUM STRENGTH ALERTNESS AID" or generic name "Caffeine"

    NDCBrand NameGeneric Name
    0363-3440AwakeCaffeine
    21130-944AwakeCaffeine
    0363-5009CaffeineCaffeine
    24385-601Good Neighbor Pharmacy Stay AwakeCaffeine
    0113-0409good sense stay awakeCaffeine
    15579-201JET ALERT Regular StrengthCAFFEINE
    0067-2070NoDozCaffeine
    15127-226Stay AlertCaffeine
    0363-0226Stay AwakeCaffeine
    0904-7955Stay AwakeCaffeine
    11822-0691Stay AwakeCaffeine
    11822-2260stay awakecaffeine
    21130-226Stay AwakeCaffeine
    30142-409stay awakeCaffeine
    30142-726Stay AwakeCaffeine

    Trademark Results [NoDoz]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    NODOZ
    NODOZ
    85644375 4498772 Live/Registered
    LIL' DRUG STORE PRODUCTS, INC.
    2012-06-06
    NODOZ
    NODOZ
    85413816 4121899 Live/Registered
    LIL' DRUG STORE PRODUCTS, INC.
    2011-09-02
    NODOZ
    NODOZ
    77494974 not registered Dead/Abandoned
    Novartis AG
    2008-06-10
    NODOZ
    NODOZ
    72194027 0792839 Live/Registered
    BRISTOL-MYERS COMPANY
    1964-05-22
    NODOZ
    NODOZ
    71597610 0545634 Dead/Expired
    HARRISON PRODUCTS, INC.
    1950-05-17

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