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    NDC 71399-7889-01 Magnesium Citrate 1.745 g/29.6mL Details

    Magnesium Citrate 1.745 g/29.6mL

    Magnesium Citrate is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by AKRON PHARMA INC. The primary component is MAGNESIUM CITRATE.

    Product Information

    NDC 71399-7889
    Product ID 71399-7889_ba8443ea-0109-4b71-a471-7d0fa021757b
    Associated GPIs
    GCN Sequence Number 003025
    GCN Sequence Number Description magnesium citrate SOLUTION ORAL
    HIC3 D6S
    HIC3 Description LAXATIVES AND CATHARTICS
    GCN 09240
    HICL Sequence Number 001328
    HICL Sequence Number Description MAGNESIUM CITRATE
    Brand/Generic Generic
    Proprietary Name Magnesium Citrate
    Proprietary Name Suffix Saline Laxative
    Non-Proprietary Name Magnesium citrate
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 1.745
    Active Ingredient Units g/29.6mL
    Substance Name MAGNESIUM CITRATE
    Labeler Name AKRON PHARMA INC
    Pharmaceutical Class Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part334
    Listing Certified Through 2024-12-31

    Package

    NDC 71399-7889-01 (71399788901)

    NDC Package Code 71399-7889-1
    Billing NDC 71399788901
    Package 296 mL in 1 BOTTLE (71399-7889-1)
    Marketing Start Date 2023-01-02
    NDC Exclude Flag N
    Pricing Information N/A