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    NDC 70518-0028-00 ENALAPRIL MALEATE 20 mg/1 Details

    ENALAPRIL MALEATE 20 mg/1

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

    Product Information

    NDC 70518-0028
    Product ID 70518-0028_0e0cd179-8678-d1a5-e063-6294a90a7ff8
    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 ENALAPRIL MALEATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name ENALAPRIL MALEATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ENALAPRIL MALEATE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075483
    Listing Certified Through 2025-12-31

    Package

    NDC 70518-0028-00 (70518002800)

    NDC Package Code 70518-0028-0
    Billing NDC 70518002800
    Package 90 TABLET in 1 BOTTLE (70518-0028-0)
    Marketing Start Date 2016-12-01
    NDC Exclude Flag N
    Pricing Information N/A