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    NDC 72854-0233-20 Mucinex Nightshift Cold and Flu 325; 10; 1.25 mg/1; mg/1; mg/1 Details

    Mucinex Nightshift Cold and Flu 325; 10; 1.25 mg/1; mg/1; mg/1

    Mucinex Nightshift Cold and Flu is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by RB Health (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; TRIPROLIDINE HYDROCHLORIDE.

    Product Information

    NDC 72854-0233
    Product ID 72854-233_fda420fa-f5fd-312e-e053-6394a90a2b81
    Associated GPIs 43998903300320
    GCN Sequence Number 082243
    GCN Sequence Number Description triprolidine/DM/acetaminophen TABLET 1.25-10 MG ORAL
    HIC3 B4G
    HIC3 Description NON-OPIOID ANTITUS-1ST GEN ANTIHIST-ANALGESIC COMB
    GCN 49596
    HICL Sequence Number 046405
    HICL Sequence Number Description TRIPROLIDINE HCL/DEXTROMETHORPHAN HBR/ACETAMINOPHEN
    Brand/Generic Brand
    Proprietary Name Mucinex Nightshift Cold and Flu
    Proprietary Name Suffix Maximum Strength
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 325; 10; 1.25
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; TRIPROLIDINE HYDROCHLORIDE
    Labeler Name RB Health (US) LLC
    Pharmaceutical Class Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 72854-0233-20 (72854023320)

    NDC Package Code 72854-233-20
    Billing NDC 72854023320
    Package 2 BLISTER PACK in 1 CARTON (72854-233-20) / 10 TABLET, COATED in 1 BLISTER PACK
    Marketing Start Date 2021-07-01
    NDC Exclude Flag N
    Pricing Information N/A