NDC 65597-114

Tribenzor

Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide

Tribenzor is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Daiichi Sankyo, Inc.. The primary component is Olmesartan Medoxomil; Amlodipine Besylate; Hydrochlorothiazide.

Product ID65597-114_11604411-5117-4e54-892d-9709c6d39e6a
NDC65597-114
Product TypeHuman Prescription Drug
Proprietary NameTribenzor
Generic NameOlmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-07-31
Marketing CategoryNDA / NDA
Application NumberNDA200175
Labeler NameDaiichi Sankyo, Inc.
Substance NameOLMESARTAN MEDOXOMIL; AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE
Active Ingredient Strength20 mg/1; mg/1; mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 65597-114-07

7 TABLET, FILM COATED in 1 BOTTLE (65597-114-07)
Marketing Start Date2010-07-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65597-114-07 [65597011407]

Tribenzor TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200175
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-31

NDC 65597-114-10 [65597011410]

Tribenzor TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200175
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-31

NDC 65597-114-70 [65597011470]

Tribenzor TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200175
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-31

NDC 65597-114-90 [65597011490]

Tribenzor TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200175
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-07-31

NDC 65597-114-30 [65597011430]

Tribenzor TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200175
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-07-31

Drug Details

Active Ingredients

IngredientStrength
OLMESARTAN MEDOXOMIL20 mg/1

OpenFDA Data

SPL SET ID:5562b3f5-8757-11de-8a39-0800200c9a66
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 999995
  • 1000005
  • 1000000
  • 999967
  • 999971
  • 999991
  • 999990
  • 1000001
  • 999986
  • 999996
  • UPC Code
  • 0365597114302
  • 0365597118904
  • 0365597115309
  • 0365597116306
  • 0365597117303
  • Pharmacological Class

    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]
    • Calcium Channel Antagonists [MoA]
    • Dihydropyridine Calcium Channel Blocker [EPC]
    • Dihydropyridines [CS]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    Medicade Reported Pricing

    65597011490 TRIBENZOR 20-5-12.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    65597011430 TRIBENZOR 20-5-12.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Tribenzor" or generic name "Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0713-0874Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    0713-0875Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    0713-0876Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    0713-0877Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    0713-0878Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    65597-114Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    65597-115Tribenzorolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    65597-117TribenzorTribenzor
    65597-116TribenzorTribenzor
    65597-118TribenzorTribenzor
    49884-786olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    49884-787olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    49884-788olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    49884-789olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    49884-790olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    63629-2238olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    63629-2239olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    63629-2240olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
    63629-2241olmesartan medoxomil / amlodipine besylate / hydrochlorothiazideolmesartan medoxomil / amlodipine besylate / hydrochlorothiazide

    Trademark Results [Tribenzor]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    TRIBENZOR
    TRIBENZOR
    85416907 4142005 Live/Registered
    DAIICHI SANKYO COMPANY, LIMITED
    2011-09-07
    TRIBENZOR
    TRIBENZOR
    77744208 3982012 Live/Registered
    DAIICHI SANKYO COMPANY, LIMITED
    2009-05-26

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.