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    NDC 71179-0002-21 Guaifenesin 1200 mg/1 Details

    Guaifenesin 1200 mg/1

    Guaifenesin is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by VESPYR BRANDS, INC.. The primary component is GUAIFENESIN.

    Product Information

    NDC 71179-0002
    Product ID 71179-002_8f11da6c-2f66-42cf-a7f8-d0d80ffafa61
    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 Guaifenesin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1200
    Active Ingredient Units mg/1
    Substance Name GUAIFENESIN
    Labeler Name VESPYR BRANDS, INC.
    Pharmaceutical Class Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210453
    Listing Certified Through 2024-12-31

    Package

    NDC 71179-0002-21 (71179000221)

    NDC Package Code 71179-002-21
    Billing NDC 71179000221
    Package 3 BLISTER PACK in 1 CARTON (71179-002-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2022-06-27
    NDC Exclude Flag N
    Pricing Information N/A
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