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    NDC 13668-0383-90 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/12.5 mg 10; 12.5; 40 mg/1; mg/1; mg/1 Details

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/12.5 mg 10; 12.5; 40 mg/1; mg/1; mg/1

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/12.5 mg is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 13668-0383
    Product ID 13668-383_1ae8e8eb-da85-4790-8b02-a34f95c122f0
    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, Amlodipine and Hydrochlorothiazide 40/10/12.5 mg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 40/10/12.5 mg
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10; 12.5; 40
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
    Labeler Name Torrent Pharmaceuticals Limited
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], In
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203580
    Listing Certified Through 2024-12-31

    Package

    NDC 13668-0383-90 (13668038390)

    NDC Package Code 13668-383-90
    Billing NDC 13668038390
    Package 90 TABLET in 1 BOTTLE (13668-383-90)
    Marketing Start Date 2016-10-26
    NDC Exclude Flag N
    Pricing Information N/A