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    NDC 63629-1140-01 M-Natal Plus 22; 120; 200; 2; 12; 27; 1; 20; 10; 3; 1.84; 4000; 400; 25 [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1 Details

    M-Natal Plus 22; 120; 200; 2; 12; 27; 1; 20; 10; 3; 1.84; 4000; 400; 25 [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1

    M-Natal Plus is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is .ALPHA.-TOCOPHEROL ACETATE; ASCORBIC ACID; CALCIUM; COPPER; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE; VITAMIN A; VITAMIN D; ZINC.

    Product Information

    NDC 63629-1140
    Product ID 63629-1140_d0a3976a-dc8f-4a4c-a35b-30de5afc4ba1
    Associated GPIs 78512015000324
    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 M-Natal Plus
    Proprietary Name Suffix n/a
    Non-Proprietary Name Vitamin A, Vitamin C, Vitamin D, Vitamin E, Thiamine, Riboflavin, Niacin, Vitamin B6, Folic Acid, Vitamin B12, Calcium, Iron, Zinc, Copper
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 22; 120; 200; 2; 12; 27; 1; 20; 10; 3; 1.84; 4000; 400; 25
    Active Ingredient Units [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1
    Substance Name .ALPHA.-TOCOPHEROL ACETATE; ASCORBIC ACID; CALCIUM; COPPER; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE; VITAMIN A; VITAMIN D; ZINC
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calcium [CS], Calcium [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE], Ni
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-1140-01 (63629114001)

    NDC Package Code 63629-1140-1
    Billing NDC 63629114001
    Package 100 TABLET in 1 BOTTLE (63629-1140-1)
    Marketing Start Date 2020-10-06
    NDC Exclude Flag N
    Pricing Information N/A