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    NDC 17856-0155-01 Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution 15; 6.25 mg/5mL; mg/5mL Details

    Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution 15; 6.25 mg/5mL; mg/5mL

    Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ATLANTIC BIOLOGICALS CORP.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE.

    Product Information

    NDC 17856-0155
    Product ID 17856-0155_1902518a-023e-45aa-8a10-d64fdbf94827
    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 Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution
    Proprietary Name Suffix n/a
    Non-Proprietary Name Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 15; 6.25
    Active Ingredient Units mg/5mL; mg/5mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; PROMETHAZINE HYDROCHLORIDE
    Labeler Name ATLANTIC BIOLOGICALS CORP.
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS], 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 ANDA
    Application Number ANDA040649
    Listing Certified Through 2024-12-31

    Package

    NDC 17856-0155-01 (17856015501)

    NDC Package Code 17856-0155-1
    Billing NDC 17856015501
    Package 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0155-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0155-2)
    Marketing Start Date 2023-09-13
    NDC Exclude Flag N
    Pricing Information N/A