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    NDC 71335-0257-04 Terbinafine Hydrochloride 250 mg/1 Details

    Terbinafine Hydrochloride 250 mg/1

    Terbinafine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is TERBINAFINE HYDROCHLORIDE.

    Product Information

    NDC 71335-0257
    Product ID 71335-0257_3a257a4c-a138-4c53-a14b-940adeeb84d5
    Associated GPIs 11000080100310
    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 Terbinafine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Terbinafine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name TERBINAFINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Allylamine Antifungal [EPC], Allylamine [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077137
    Listing Certified Through 2022-12-31

    Package

    NDC 71335-0257-04 (71335025704)

    NDC Package Code 71335-0257-4
    Billing NDC 71335025704
    Package 100 TABLET in 1 BOTTLE (71335-0257-4)
    Marketing Start Date 2015-06-12
    NDC Exclude Flag N
    Pricing Information N/A