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    NDC 71335-1668-08 Terbinafine 250 mg/1 Details

    Terbinafine 250 mg/1

    Terbinafine 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 71335-1668
    Product ID 71335-1668_7b05bf8b-12ea-4724-8da3-78520e99f7fe
    Associated GPIs
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Terbinafine
    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 ANDA077533
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1668-08 (71335166808)

    NDC Package Code 71335-1668-8
    Billing NDC 71335166808
    Package 14 TABLET in 1 BOTTLE (71335-1668-8)
    Marketing Start Date 2020-08-10
    NDC Exclude Flag N
    Pricing Information N/A