Search by Drug Name or NDC

    NDC 00135-0246-01 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 00135-0246
    Product ID 0135-0246_06065f63-3c3b-43b0-ae01-18e1d7447b28
    Associated GPIs 48300010000520
    GCN Sequence Number 002690
    GCN Sequence Number Description calcium carbonate TAB CHEW 300MG(750) ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 07894
    HICL Sequence Number 001163
    HICL Sequence Number Description CALCIUM CARBONATE
    Brand/Generic Brand
    Proprietary Name TUMS
    Proprietary Name Suffix Smoothies
    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 00135-0246-01 (00135024601)

    NDC Package Code 0135-0246-01
    Billing NDC 00135024601
    Package 12 TABLET, CHEWABLE in 1 CELLO PACK (0135-0246-01)
    Marketing Start Date 2010-03-24
    NDC Exclude Flag N
    Pricing Information N/A