Search by Drug Name or NDC

    NDC 71335-1668-09 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 71335-1668-09 (71335166809)

    NDC Package Code 71335-1668-9
    Billing NDC 71335166809
    Package 28 TABLET in 1 BOTTLE (71335-1668-9)
    Marketing Start Date 2022-02-14
    NDC Exclude Flag N
    Pricing Information N/A