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    NDC 63629-7115-05 Mucinex 600 mg/1 Details

    Mucinex 600 mg/1

    Mucinex is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is GUAIFENESIN.

    Product Information

    NDC 63629-7115
    Product ID 63629-7115_754211c8-8a60-4d70-b7ca-61f6def1e53f
    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 Mucinex
    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 Bryant Ranch Prepack
    Pharmaceutical Class Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021282
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-7115-05 (63629711505)

    NDC Package Code 63629-7115-5
    Billing NDC 63629711505
    Package 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-5)
    Marketing Start Date 2022-09-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 63629-7115-04 63629-7116-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL a898b584-e17e-45c4-8a28-9f686b95dca0 Details

    Revised: 9/2022
    Document Id: 754211c8-8a60-4d70-b7ca-61f6def1e53f
    Set id: a898b584-e17e-45c4-8a28-9f686b95dca0
    Version: 10
    Effective Time: 20220901