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    NDC 59088-0165-54 Vitrexyl plus Iron 30; 120; 200; 20; 35; 8; 27; 1000; 200; 2.3; 45; 20; 20; 3.4; 55; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1 Details

    Vitrexyl plus Iron 30; 120; 200; 20; 35; 8; 27; 1000; 200; 2.3; 45; 20; 20; 3.4; 55; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1

    Vitrexyl plus Iron is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELEN.

    Product Information

    NDC 59088-0165
    Product ID 59088-165_f2047f00-c3fe-3e18-e053-2a95a90af35f
    Associated GPIs 78310000000300
    GCN Sequence Number 081657
    GCN Sequence Number Description mv-mn no.86/iron/folic acid TABLET 27 MG-1 MG ORAL
    HIC3 C6Z
    HIC3 Description MULTIVITAMIN PREPARATIONS
    GCN 48808
    HICL Sequence Number 046955
    HICL Sequence Number Description MULTIVITAMIN WITH MINERALS NO.86/FERROUS FUMARATE/FOLIC ACID
    Brand/Generic Brand
    Proprietary Name Vitrexyl plus Iron
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ferrous Fumarate, Folic Acid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 30; 120; 200; 20; 35; 8; 27; 1000; 200; 2.3; 45; 20; 20; 3.4; 55; 3; 1500; 25
    Active Ingredient Units mg/1; mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1
    Substance Name .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELEN
    Labeler Name PureTek Corporation
    Pharmaceutical Class Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagul
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 59088-0165-54 (59088016554)

    NDC Package Code 59088-165-54
    Billing NDC 59088016554
    Package 30 TABLET in 1 BOTTLE, PLASTIC (59088-165-54)
    Marketing Start Date 2020-08-24
    NDC Exclude Flag N
    Pricing Information N/A
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