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    NDC 43598-0110-01 Guaifenesin 600 mg 600 mg/1 Details

    Guaifenesin 600 mg 600 mg/1

    Guaifenesin 600 mg is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Dr. Reddy's Laboratories Inc.. The primary component is GUAIFENESIN.

    Product Information

    NDC 43598-0110
    Product ID 43598-110_aef9a93b-9bb3-7b51-f163-14c2469872cf
    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 600 mg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 600
    Active Ingredient Units mg/1
    Substance Name GUAIFENESIN
    Labeler Name Dr. Reddy's Laboratories Inc.
    Pharmaceutical Class Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215932
    Listing Certified Through 2024-12-31

    Package

    NDC 43598-0110-01 (43598011001)

    NDC Package Code 43598-110-01
    Billing NDC 43598011001
    Package 5 BLISTER PACK in 1 CARTON (43598-110-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2022-09-01
    NDC Exclude Flag N
    Pricing Information N/A