Search by Drug Name or NDC

    NDC 00135-0540-01 TUMS 1000 mg/1 Details

    TUMS 1000 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 00135-0540
    Product ID 0135-0540_4618db68-f98f-42e1-ade3-23cc4fdad7d6
    Associated GPIs
    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 ULTRA
    Non-Proprietary Name calcium carbonate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 1000
    Active Ingredient Units mg/1
    Substance Name CALCIUM CARBONATE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M001
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0540-01 (00135054001)

    NDC Package Code 0135-0540-01
    Billing NDC 00135054001
    Package 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0540-01)
    Marketing Start Date 2010-02-12
    NDC Exclude Flag N
    Pricing Information N/A