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    NDC 71205-0853-55 Benzonatate 100 mg/1 Details

    Benzonatate 100 mg/1

    Benzonatate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is BENZONATATE.

    Product Information

    NDC 71205-0853
    Product ID 71205-853_45d9b32a-3198-49d5-addf-f077fec50b9c
    Associated GPIs 43102010000105
    GCN Sequence Number 004641
    GCN Sequence Number Description benzonatate CAPSULE 100 MG ORAL
    HIC3 H6C
    HIC3 Description ANTITUSSIVES, NON-OPIOID
    GCN 29840
    HICL Sequence Number 001929
    HICL Sequence Number Description BENZONATATE
    Brand/Generic Generic
    Proprietary Name Benzonatate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Benzonatate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name BENZONATATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211518
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0853-55 (71205085355)

    NDC Package Code 71205-853-55
    Billing NDC 71205085355
    Package 500 CAPSULE in 1 BOTTLE (71205-853-55)
    Marketing Start Date 2022-06-20
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 45d9b32a-3198-49d5-addf-f077fec50b9c Details

    Revised: 6/2022