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    NDC 71205-0605-21 Benzonatate 200 mg/1 Details

    Benzonatate 200 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 71205-0605
    Product ID 71205-605_2fae3438-3fe9-4f4f-bd89-35fb7050c560
    Associated GPIs 43102010000110
    GCN Sequence Number 044168
    GCN Sequence Number Description benzonatate CAPSULE 200 MG ORAL
    HIC3 H6C
    HIC3 Description ANTITUSSIVES, NON-OPIOID
    GCN 93007
    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 200
    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 ANDA081297
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0605-21 (71205060521)

    NDC Package Code 71205-605-21
    Billing NDC 71205060521
    Package 21 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-21)
    Marketing Start Date 2021-09-15
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL bc435603-ddc4-4083-af09-2e562defbe7f Details

    Revised: 5/2022