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    NDC 68788-7309-03 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 Preferred Pharmaceuticals Inc.. The primary component is ENALAPRIL MALEATE.

    Product Information

    NDC 68788-7309
    Product ID 68788-7309_112ae2b7-6d20-4d53-9f28-8a6721d90240
    Associated GPIs 36100020100315
    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 Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA018998
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7309-03 (68788730903)

    NDC Package Code 68788-7309-3
    Billing NDC 68788730903
    Package 30 TABLET in 1 BOTTLE (68788-7309-3)
    Marketing Start Date 2019-01-04
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 2e4e0a42-e09d-4b58-b0de-4044d1dfbab7 Details

    Revised: 5/2022