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    NDC 13925-0118-90 Se-Tan PLUS 10; .8; 15; 162; 1; 115.2; 1.3; 30; 5; 6; 200; 10; 18.2 mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1 Details

    Se-Tan PLUS 10; .8; 15; 162; 1; 115.2; 1.3; 30; 5; 6; 200; 10; 18.2 mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1

    Se-Tan PLUS is a ORAL CAPSULE, GELATIN COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Seton Pharmaceuticals. The primary component is CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IRON DEXTRAN; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE.

    Product Information

    NDC 13925-0118
    Product ID 13925-118_f433b534-24d5-4608-ba84-cd904b0bc385
    Associated GPIs 82992008600130
    GCN Sequence Number 060711
    GCN Sequence Number Description iron fm,ps no.1/folic/mv no.18 CAPSULE 106 MG-1MG ORAL
    HIC3 C3B
    HIC3 Description IRON REPLACEMENT
    GCN 26937
    HICL Sequence Number 033611
    HICL Sequence Number Description IRON FUMARATE-IRON POLYSACCH CPLEX/FOLIC ACID/MULTIVIT NO.18
    Brand/Generic Generic
    Proprietary Name Se-Tan PLUS
    Proprietary Name Suffix n/a
    Non-Proprietary Name MULTIVITAMIN/MINERAL
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, GELATIN COATED
    Route ORAL
    Active Ingredient Strength 10; .8; 15; 162; 1; 115.2; 1.3; 30; 5; 6; 200; 10; 18.2
    Active Ingredient Units mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1
    Substance Name CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IRON DEXTRAN; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE
    Labeler Name Seton Pharmaceuticals
    Pharmaceutical Class Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Iron [CS], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC], Parenteral Iron Replacement [
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2023-12-31

    Package

    NDC 13925-0118-90 (13925011890)

    NDC Package Code 13925-118-90
    Billing NDC 13925011890
    Package 90 CAPSULE, GELATIN COATED in 1 BOTTLE (13925-118-90)
    Marketing Start Date 2009-10-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 56e912df-3a49-4405-8df1-7b80d12bd920 Details

    Revised: 5/2022