Search by Drug Name or NDC

    NDC 71205-0632-21 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 71205-0632
    Product ID 71205-632_a449d609-2233-477e-bdb7-df2c84a1b495
    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 ANDA206948
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0632-21 (71205063221)

    NDC Package Code 71205-632-21
    Billing NDC 71205063221
    Package 21 CAPSULE in 1 BOTTLE (71205-632-21)
    Marketing Start Date 2022-01-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 46b4f05c-9261-42fc-a016-c99eebab5646 Details

    Revised: 5/2022