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    NDC 59088-0659-31 Livita Adults 20.1; 200; 30; 200; 5; 10; 200; 500; 1000; 100; 2.4; 8; 1.7; 1.3; 1.2; 900; 2 mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; ug/mL; mg/mL Details

    Livita Adults 20.1; 200; 30; 200; 5; 10; 200; 500; 1000; 100; 2.4; 8; 1.7; 1.3; 1.2; 900; 2 mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; ug/mL; mg/mL

    Livita Adults is a ORAL LIQUID in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is .ALPHA.-TOCOPHEROL ACETATE, D-; ASCORBIC ACID; BIOTIN; CALCIUM CITRATE; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; INULIN; LEVOMEFOLATE CALCIUM; MAGNESIUM CITRATE; METHYLCOBALAMIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMIN.

    Product Information

    NDC 59088-0659
    Product ID 59088-659_0ccf48d9-b6ef-d809-e063-6294a90ab507
    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 Livita Adults
    Proprietary Name Suffix n/a
    Non-Proprietary Name Folate, Multivitamin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 20.1; 200; 30; 200; 5; 10; 200; 500; 1000; 100; 2.4; 8; 1.7; 1.3; 1.2; 900; 2
    Active Ingredient Units mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; mg/mL; ug/mL; mg/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; ug/mL; mg/mL
    Substance Name .ALPHA.-TOCOPHEROL ACETATE, D-; ASCORBIC ACID; BIOTIN; CALCIUM CITRATE; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; INULIN; LEVOMEFOLATE CALCIUM; MAGNESIUM CITRATE; METHYLCOBALAMIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMIN
    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], Folate Analog [E
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 59088-0659-31 (59088065931)

    NDC Package Code 59088-659-31
    Billing NDC 59088065931
    Package 480 mL in 1 BOTTLE (59088-659-31)
    Marketing Start Date 2023-12-15
    NDC Exclude Flag N
    Pricing Information N/A
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