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    NDC 68788-7450-03 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 Preferred Pharmaceuticals, Inc.. The primary component is TERBINAFINE HYDROCHLORIDE.

    Product Information

    NDC 68788-7450
    Product ID 68788-7450_5cc27987-281a-4eb9-ad7c-cda32888d892
    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
    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 Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Allylamine Antifungal [EPC], Allylamine [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078297
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7450-03 (68788745003)

    NDC Package Code 68788-7450-3
    Billing NDC 68788745003
    Package 30 TABLET in 1 BOTTLE (68788-7450-3)
    Marketing Start Date 2019-12-27
    NDC Exclude Flag N
    Pricing Information N/A