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    NDC 73581-0401-02 MUCUS RELIEF 600 mg/1 Details

    MUCUS RELIEF 600 mg/1

    MUCUS RELIEF is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by YYBA CORP. The primary component is GUAIFENESIN.

    Product Information

    NDC 73581-0401
    Product ID 73581-401_0e1352bf-9971-edc9-e063-6394a90adc7d
    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 MUCUS RELIEF
    Proprietary Name Suffix GUAIFENESIN EXTENDED-RELEASE 600 mg
    Non-Proprietary Name GUAIFENESIN
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GUAIFENESIN
    Labeler Name YYBA CORP
    Pharmaceutical Class Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213420
    Listing Certified Through 2025-12-31

    Package

    NDC 73581-0401-02 (73581040102)

    NDC Package Code 73581-401-02
    Billing NDC 73581040102
    Package 200 TABLET in 1 BOTTLE (73581-401-02)
    Marketing Start Date 2022-03-02
    NDC Exclude Flag N
    Pricing Information N/A