NDC 0135-0140

TUMS EX

Calcium Carbonate

TUMS EX is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Calcium Carbonate.

Product ID0135-0140_41e2252e-44ff-47d2-b035-a9b725ff1b28
NDC0135-0140
Product TypeHuman Otc Drug
Proprietary NameTUMS EX
Generic NameCalcium Carbonate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-01-18
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart331
Labeler NameGlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance NameCALCIUM CARBONATE
Active Ingredient Strength750 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0135-0140-01

8 TABLET in 1 PACKAGE (0135-0140-01)
Marketing Start Date2010-01-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0135-0140-03 [00135014003]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-01-18
Marketing End Date2018-09-30
Inactivation Date2020-01-31
Reactivation Date2020-02-28

NDC 0135-0140-02 [00135014002]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Inactivation Date2020-01-31
Reactivation Date2020-02-28

NDC 0135-0140-07 [00135014007]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Marketing End Date2011-12-10

NDC 0135-0140-05 [00135014005]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Inactivation Date2020-01-31
Reactivation Date2020-02-28

NDC 0135-0140-08 [00135014008]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Marketing End Date2011-12-10

NDC 0135-0140-04 [00135014004]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Marketing End Date2011-12-10

NDC 0135-0140-09 [00135014009]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Marketing End Date2011-12-10

NDC 0135-0140-06 [00135014006]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Marketing End Date2011-12-10

NDC 0135-0140-10 [00135014010]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-18
Inactivation Date2020-01-31
Reactivation Date2020-02-28

NDC 0135-0140-01 [00135014001]

TUMS EX TABLET
Marketing CategoryOTC monograph final
Application Numberpart331
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-01-18
Inactivation Date2020-01-31
Reactivation Date2020-02-28

Drug Details

Active Ingredients

IngredientStrength
CALCIUM CARBONATE750 mg/1

OpenFDA Data

SPL SET ID:593a0494-d669-4bcf-8412-b92645b2d76c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 308915
  • 1044532

    • NDC Crossover Matching brand name "TUMS EX" or generic name "Calcium Carbonate"

    NDCBrand NameGeneric Name
    0135-0521TUMS EXTUMS EX
    0113-7489basic care antacidCalcium carbonate
    0113-7595basic care antacidCalcium Carbonate
    0054-3117Calcium CarbonateCalcium Carbonate
    0054-4120Calcium CarbonateCalcium Carbonate
    0054-8120Calcium CarbonateCalcium Carbonate
    0121-0766Calcium CarbonateCalcium Carbonate
    0121-4766Calcium CarbonateCalcium Carbonate
    0113-0009Good Sense Antacidcalcium carbonate
    0113-0179good sense antacidCalcium carbonate
    0113-0468good sense antacidCalcium carbonate
    0113-0478good sense antacidcalcium carbonate
    0113-0485good sense antacidcalcium carbonate
    0113-0489good sense antacidCalcium carbonate
    0113-0595good sense antacidCalcium Carbonate
    0113-0881Good Sense Antacidcalcium carbonate
    0113-0904good sense antacidCalcium carbonate
    0113-0962good sense antacidCalcium carbonate
    0135-0070TUMScalcium carbonate
    0135-0071TUMScalcium carbonate
    0135-0074TUMScalcium carbonate
    0135-0076TUMScalcium carbonate
    0135-0118TUMScalcium carbonate
    0135-0140TUMScalcium carbonate
    0135-0154TUMScalcium carbonate
    0135-0155TUMScalcium carbonate
    0135-0178TUMScalcium carbonate

    Trademark Results [TUMS]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    TUMS
    TUMS
    98794008 not registered Live/Pending
    Haleon US IP LLC
    2024-10-10
    TUMS
    TUMS
    98058821 not registered Live/Pending
    BANG, Hai Hwa
    2023-06-26
    TUMS
    TUMS
    79373831 not registered Live/Pending
    BANG, Hai Hwa
    2023-05-30
    TUMS
    TUMS
    78226130 not registered Dead/Abandoned
    SmithKline Beecham Corporation
    2003-03-17
    TUMS
    TUMS
    77619345 3741016 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    2008-11-21
    TUMS
    TUMS
    77155155 not registered Dead/Abandoned
    GLAXOSMITHKLINE LLC
    2007-04-12
    TUMS
    TUMS
    75696786 not registered Dead/Abandoned
    SmithKline Beecham Corporation
    1999-05-03
    TUMS
    TUMS
    75676521 2441507 Dead/Cancelled
    GLAXOSMITHKLINE LLC
    1999-04-07
    TUMS
    TUMS
    75465207 2240777 Dead/Cancelled
    SmithKline Beecham Corporation
    1998-04-09
    TUMS
    TUMS
    75058334 2076469 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US)
    1996-02-15
    TUMS
    TUMS
    74723028 1979916 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    1995-08-30
    TUMS
    TUMS
    74722865 1979915 Live/Registered
    GLAXOSMITHKLINE CONSUMER HEALTHCARE (US) IP LLC
    1995-08-30
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