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    NDC 00363-0713-33 Acid Reducer Complete 800; 10; 165 mg/1; mg/1; mg/1 Details

    Acid Reducer Complete 800; 10; 165 mg/1; mg/1; mg/1

    Acid Reducer Complete is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE.

    Product Information

    NDC 00363-0713
    Product ID 0363-0713_02b59032-b352-4001-8be0-a2683fad38e7
    Associated GPIs 47300010001805
    GCN Sequence Number 002858
    GCN Sequence Number Description bismuth subsalicylate ORAL SUSP 262MG/15ML ORAL
    HIC3 D6D
    HIC3 Description ANTIDIARRHEALS
    GCN 26970
    HICL Sequence Number 001246
    HICL Sequence Number Description BISMUTH SUBSALICYLATE
    Brand/Generic Generic
    Proprietary Name Acid Reducer Complete
    Proprietary Name Suffix n/a
    Non-Proprietary Name Famotidine, Calcium Carbonate, 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 Walgreen Company
    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 00363-0713-33 (00363071333)

    NDC Package Code 0363-0713-33
    Billing NDC 00363071333
    Package 60 TABLET, CHEWABLE in 1 BOTTLE (0363-0713-33)
    Marketing Start Date 2018-11-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6f1dcfda-c12a-4c3b-80a2-c9e15517c88f Details

    Revised: 7/2022