Search by Drug Name or NDC

    NDC 59088-0660-16 Livita Children 10; 66.67; 10; 66.67; 1.67; 3.33; 66.67; 166.67; 333; 33.33; .8; 2.67; .57; .43; .4; 300; .67 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 Children 10; 66.67; 10; 66.67; 1.67; 3.33; 66.67; 166.67; 333; 33.33; .8; 2.67; .57; .43; .4; 300; .67 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 Children 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 59088-0660
    Product ID 59088-660_0ca12bbf-0b01-3432-e063-6294a90a8c45
    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 Children
    Proprietary Name Suffix n/a
    Non-Proprietary Name Folate, Multivitamin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 10; 66.67; 10; 66.67; 1.67; 3.33; 66.67; 166.67; 333; 33.33; .8; 2.67; .57; .43; .4; 300; .67
    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 59088-0660-16 (59088066016)

    NDC Package Code 59088-660-16
    Billing NDC 59088066016
    Package 237 mL in 1 BOTTLE (59088-660-16)
    Marketing Start Date 2023-12-18
    NDC Exclude Flag N
    Pricing Information N/A
    << 59088-0659-31 59088-0685-52 >>

    Contents