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    NDC 71335-1836-09 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 71335-1836
    Product ID 71335-1836_4d8e2da8-b9c3-4b8b-97e1-e24e0d745495
    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 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 ANDA078163
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1836-09 (71335183609)

    NDC Package Code 71335-1836-9
    Billing NDC 71335183609
    Package 28 TABLET in 1 BOTTLE, PLASTIC (71335-1836-9)
    Marketing Start Date 2022-02-14
    NDC Exclude Flag N
    Pricing Information N/A