Search by Drug Name or NDC

    NDC 13668-0382-05 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/25 mg 10; 25; 40 mg/1; mg/1; mg/1 Details

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/25 mg 10; 25; 40 mg/1; mg/1; mg/1

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/25 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 13668-0382
    Product ID 13668-382_1ae8e8eb-da85-4790-8b02-a34f95c122f0
    Associated GPIs 36994503450350
    GCN Sequence Number 066542
    GCN Sequence Number Description olmesartan/amlodipin/hcthiazid TABLET 40-10-25MG ORAL
    HIC3 A4V
    HIC3 Description ANGIOTEN.RECEPTR ANTAG-CALCIUM CHANL BLKR-THIAZIDE
    GCN 28855
    HICL Sequence Number 037089
    HICL Sequence Number Description OLMESARTAN MEDOXOMIL/AMLODIPINE BESYLATE/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/10/25 mg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 40/10/25 mg
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10; 25; 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 13668-0382-05 (13668038205)

    NDC Package Code 13668-382-05
    Billing NDC 13668038205
    Package 500 TABLET in 1 BOTTLE (13668-382-05)
    Marketing Start Date 2016-10-26
    NDC Exclude Flag N
    Pricing Information N/A