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    NDC 50967-0219-90 NESTABS 30; 45; 155; 450; 55; 10; 32; 1; 20; 100; 50; 3; 120; 3; 10 [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1 Details

    NESTABS 30; 45; 155; 450; 55; 10; 32; 1; 20; 100; 50; 3; 120; 3; 10 [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1

    NESTABS is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by WOMENS CHOICE PHARMACEUTICALS LLC. The primary component is .ALPHA.-TOCOPHEROL ACETATE, D-; CALCIUM CARBONATE; CALCIUM FORMATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CYANOCOBALAMIN; FERROUS BISGLYCINATE; FOLIC ACID; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONO.

    Product Information

    NDC 50967-0219
    Product ID 50967-219_f28ee215-1dc9-0062-e053-2995a90a6c14
    Associated GPIs 78512066000340
    GCN Sequence Number 067006
    GCN Sequence Number Description prenatal vit86/iron/folic acid TABLET 32 MG-1 MG ORAL
    HIC3 C6F
    HIC3 Description PRENATAL VITAMIN PREPARATIONS
    GCN 29455
    HICL Sequence Number 037363
    HICL Sequence Number Description PRENATAL VITAMIN NO.86/IRON BIS-GLYCINATE/FOLIC ACID
    Brand/Generic Brand
    Proprietary Name NESTABS
    Proprietary Name Suffix Prenatal Multi-vitamin/Mineral Supplement
    Non-Proprietary Name Multi-vitamin/Mineral Supplement with Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous (II) bis-Glycinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 30; 45; 155; 450; 55; 10; 32; 1; 20; 100; 50; 3; 120; 3; 10
    Active Ingredient Units [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1
    Substance Name .ALPHA.-TOCOPHEROL ACETATE, D-; CALCIUM CARBONATE; CALCIUM FORMATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CYANOCOBALAMIN; FERROUS BISGLYCINATE; FOLIC ACID; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONO
    Labeler Name WOMENS CHOICE PHARMACEUTICALS LLC
    Pharmaceutical Class Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Cations, Divalent [CS], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 50967-0219-90 (50967021990)

    NDC Package Code 50967-219-90
    Billing NDC 50967021990
    Package 1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50967-219-90)
    Marketing Start Date 2011-02-01
    NDC Exclude Flag N
    Pricing Information N/A