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    NDC 53002-1129-00 verapamil hydrochloride 240 mg/1 Details

    verapamil hydrochloride 240 mg/1

    verapamil hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is VERAPAMIL HYDROCHLORIDE.

    Product Information

    NDC 53002-1129
    Product ID 53002-1129_ff572f24-9420-4ac1-8ccf-e5db94e435d4
    Associated GPIs 34000030100420
    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, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 240
    Active Ingredient Units mg/1
    Substance Name VERAPAMIL HYDROCHLORIDE
    Labeler Name RPK Pharmaceuticals, 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 ANDA078906
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1129-00 (53002112900)

    NDC Package Code 53002-1129-0
    Billing NDC 53002112900
    Package 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-1129-0)
    Marketing Start Date 2018-10-01
    NDC Exclude Flag N
    Pricing Information N/A