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    NDC 00135-0155-01 TUMS 750 mg/1 Details

    TUMS 750 mg/1

    TUMS is a ORAL TABLET, CHEWABLE 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 Information

    NDC 00135-0155
    Product ID 0135-0155_c01ac048-a94e-494f-adbc-95bbf7497fc0
    Associated GPIs 48300010000520
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name TUMS
    Proprietary Name Suffix Extra Strength Sugar-Free
    Non-Proprietary Name calcium carbonate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name CALCIUM CARBONATE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part331
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0155-01 (00135015501)

    NDC Package Code 0135-0155-01
    Billing NDC 00135015501
    Package 80 TABLET, CHEWABLE in 1 BOTTLE (0135-0155-01)
    Marketing Start Date 2018-03-18
    NDC Exclude Flag N
    Pricing Information N/A