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    NDC 51660-0072-86 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 OHM LABORATORIES INC. The primary component is GUAIFENESIN.

    Product Information

    NDC 51660-0072
    Product ID 51660-072_a5058557-c2c7-4537-a94a-0043c782fb5b
    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 Extended Release
    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 OHM LABORATORIES INC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021282
    Listing Certified Through 2022-12-31

    Package

    NDC 51660-0072-86 (51660007286)

    NDC Package Code 51660-072-86
    Billing NDC 51660007286
    Package 2 BLISTER PACK in 1 CARTON (51660-072-86) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2017-12-10
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 4c3a3e52-6bac-4039-bb20-51ea85fbff31 Details

    Revised: 11/2018