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    NDC 68462-0438-11 Olmesartan Medoxomil 40 mg/1 Details

    Olmesartan Medoxomil 40 mg/1

    Olmesartan Medoxomil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., USA. The primary component is OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 68462-0438
    Product ID 68462-438_aa9a7b83-61b7-40c9-9fa0-4d627324b7bc
    Associated GPIs 36150055200360
    GCN Sequence Number 050290
    GCN Sequence Number Description olmesartan medoxomil TABLET 40 MG ORAL
    HIC3 A4F
    HIC3 Description ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST
    GCN 17286
    HICL Sequence Number 023490
    HICL Sequence Number Description OLMESARTAN MEDOXOMIL
    Brand/Generic Generic
    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 40
    Active Ingredient Units mg/1
    Substance Name OLMESARTAN MEDOXOMIL
    Labeler Name Glenmark Pharmaceuticals Inc., USA
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203281
    Listing Certified Through 2024-12-31

    Package

    NDC 68462-0438-11 (68462043811)

    NDC Package Code 68462-438-11
    Billing NDC 68462043811
    Package 10 BLISTER PACK in 1 CARTON (68462-438-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2017-05-25
    NDC Exclude Flag N
    Pricing Information N/A