Search by Drug Name or NDC

    NDC 13668-0397-90 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg 5; 12.5; 20 mg/1; mg/1; mg/1 Details

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg 5; 12.5; 20 mg/1; mg/1; mg/1

    Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 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 13668-0397
    Product ID 13668-397_1ae8e8eb-da85-4790-8b02-a34f95c122f0
    Associated GPIs 36994503450310
    GCN Sequence Number 066538
    GCN Sequence Number Description olmesartan/amlodipin/hcthiazid TABLET 20-5-12.5 ORAL
    HIC3 A4V
    HIC3 Description ANGIOTEN.RECEPTR ANTAG-CALCIUM CHANL BLKR-THIAZIDE
    GCN 28837
    HICL Sequence Number 037089
    HICL Sequence Number Description OLMESARTAN MEDOXOMIL/AMLODIPINE BESYLATE/HYDROCHLOROTHIAZIDE
    Brand/Generic Generic
    Proprietary Name Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 20/5/12.5 mg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tablet 20/5/12.5 mg
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5; 12.5; 20
    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 13668-0397-90 (13668039790)

    NDC Package Code 13668-397-90
    Billing NDC 13668039790
    Package 90 TABLET in 1 BOTTLE (13668-397-90)
    Marketing Start Date 2016-10-26
    NDC Exclude Flag N
    Pricing Information N/A