Search by Drug Name or NDC

    NDC 70934-0675-20 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 Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is BENZONATATE.

    Product Information

    NDC 70934-0675
    Product ID 70934-675_d0113967-5d31-db35-e053-2a95a90ada42
    Associated GPIs 43102010000105
    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 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 Denton Pharma, Inc. dba Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0675-20 (70934067520)

    NDC Package Code 70934-675-20
    Billing NDC 70934067520
    Package 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-675-20)
    Marketing Start Date 2020-04-14
    NDC Exclude Flag N
    Pricing Information N/A