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    NDC 71335-0775-03 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 71335-0775
    Product ID 71335-0775_e959822e-df83-4abd-99a6-1847aafb11ba
    Associated GPIs 36150055200340
    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 ANDA207662
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0775-03 (71335077503)

    NDC Package Code 71335-0775-3
    Billing NDC 71335077503
    Package 90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3)
    Marketing Start Date 2020-07-06
    NDC Exclude Flag N
    Pricing Information N/A