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    NDC 68788-7140-03 Bismatrol 262 mg/1 Details

    Bismatrol 262 mg/1

    Bismatrol is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is BISMUTH SUBSALICYLATE.

    Product Information

    NDC 68788-7140
    Product ID 68788-7140_e09b08be-8e27-4f7c-947f-bfc3fa1ca8c6
    Associated GPIs 47300010000507
    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 Bismatrol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bismuth subsalicylate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 262
    Active Ingredient Units mg/1
    Substance Name BISMUTH SUBSALICYLATE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Bismuth [CS], Bismuth [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part335
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7140-03 (68788714003)

    NDC Package Code 68788-7140-3
    Billing NDC 68788714003
    Package 5 BLISTER PACK in 1 CARTON (68788-7140-3) / 6 TABLET, CHEWABLE in 1 BLISTER PACK
    Marketing Start Date 2018-04-19
    NDC Exclude Flag N
    Pricing Information N/A