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    NDC 71335-1074-01 Olmesartan Medoxomil 20 mg/1 Details

    Olmesartan Medoxomil 20 mg/1

    Olmesartan Medoxomil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 71335-1074
    Product ID 71335-1074_c4b6d748-6473-4408-8e41-8def681662d2
    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 Olmesartan Medoxomil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olmesartan Medoxomil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OLMESARTAN MEDOXOMIL
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204798
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1074-01 (71335107401)

    NDC Package Code 71335-1074-1
    Billing NDC 71335107401
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71335-1074-1)
    Marketing Start Date 2019-01-14
    NDC Exclude Flag N
    Pricing Information N/A