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    NDC 70518-2184-01 VERAPAMIL HYDROCHLORIDE 80 mg/1 Details

    VERAPAMIL HYDROCHLORIDE 80 mg/1

    VERAPAMIL HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is VERAPAMIL HYDROCHLORIDE.

    Product Information

    NDC 70518-2184
    Product ID 70518-2184_feb8eafb-68f1-ec29-e053-6294a90aae77
    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 VERAPAMIL HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name VERAPAMIL HYDROCHLORIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/1
    Substance Name VERAPAMIL HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA071881
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2184-01 (70518218401)

    NDC Package Code 70518-2184-1
    Billing NDC 70518218401
    Package 100 CUP, UNIT-DOSE in 1 BOX (70518-2184-1) / 1 TABLET in 1 CUP, UNIT-DOSE (70518-2184-2)
    Marketing Start Date 2022-01-26
    NDC Exclude Flag N
    Pricing Information N/A