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    NDC 59088-0156-54 Menatrol 220; 600; 1000; 100; 1.5; 4 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1 Details

    Menatrol 220; 600; 1000; 100; 1.5; 4 mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1

    Menatrol is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is CALCIUM CARBONATE; CHOLECALCIFEROL; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; PYRIDOXINE HYDROCHLORIDE; RHUBARB.

    Product Information

    NDC 59088-0156
    Product ID 59088-156_0a100e7d-3a8e-2d8b-e063-6394a90a3203
    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 Menatrol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Folate, Multivitamin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 220; 600; 1000; 100; 1.5; 4
    Active Ingredient Units mg/1; [iU]/1; ug/1; mg/1; mg/1; mg/1
    Substance Name CALCIUM CARBONATE; CHOLECALCIFEROL; LEVOMEFOLATE CALCIUM; MAGNESIUM OXIDE; PYRIDOXINE HYDROCHLORIDE; RHUBARB
    Labeler Name PureTek Corporation
    Pharmaceutical Class Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Folate Analog [EPC], Folic Acid [CS], Inc
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 59088-0156-54 (59088015654)

    NDC Package Code 59088-156-54
    Billing NDC 59088015654
    Package 30 CAPSULE in 1 BOTTLE, PLASTIC (59088-156-54)
    Marketing Start Date 2023-12-18
    NDC Exclude Flag N
    Pricing Information N/A