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    NDC 41250-0284-71 Dual Action Complete 800; 10; 165 mg/1; mg/1; mg/1 Details

    Dual Action Complete 800; 10; 165 mg/1; mg/1; mg/1

    Dual Action Complete is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution Inc. The primary component is CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE.

    Product Information

    NDC 41250-0284
    Product ID 41250-284_50f026c2-d413-442e-872f-2627afabcecb
    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 Dual Action Complete
    Proprietary Name Suffix n/a
    Non-Proprietary Name famotidine, calcium carbonate and magnesium hydroxide
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 800; 10; 165
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
    Labeler Name Meijer Distribution Inc
    Pharmaceutical Class Calculi Dissolution Agent [EPC], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Elect
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077355
    Listing Certified Through 2024-12-31

    Package

    NDC 41250-0284-71 (41250028471)

    NDC Package Code 41250-284-71
    Billing NDC 41250028471
    Package 50 TABLET, CHEWABLE in 1 BOTTLE (41250-284-71)
    Marketing Start Date 2016-01-26
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6e8ed233-9ffb-46f7-9632-d5bc3d3a558b Details

    Revised: 7/2022