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    NDC 63629-8218-01 Amlodipine and Olmesartan Medoxomil 5; 20 mg/1; mg/1 Details

    Amlodipine and Olmesartan Medoxomil 5; 20 mg/1; mg/1

    Amlodipine and 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 AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 63629-8218
    Product ID 63629-8218_be70cfef-9e3e-448d-ac5c-641d10335d00
    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 Amlodipine and Olmesartan Medoxomil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Amlodipine and Olmesartan Medoxomil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 20
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206906
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-8218-01 (63629821801)

    NDC Package Code 63629-8218-1
    Billing NDC 63629821801
    Package 30 TABLET, FILM COATED in 1 BOTTLE (63629-8218-1)
    Marketing Start Date 2019-08-12
    NDC Exclude Flag N
    Pricing Information N/A