NDC 0093-5006

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide

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

Product ID0093-5006_020adeeb-c840-4eab-91ab-781fa292fb0f
NDC0093-5006
Product TypeHuman Prescription Drug
Proprietary NameOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Generic NameOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-11-14
Marketing CategoryANDA / ANDA
Application NumberANDA202491
Labeler NameTeva Pharmaceuticals USA, Inc.
Substance NameOLMESARTAN MEDOXOMIL; AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE
Active Ingredient Strength40 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 Through2020-12-31

Packaging

NDC 0093-5006-56

30 TABLET, FILM COATED in 1 BOTTLE (0093-5006-56)
Marketing Start Date2016-11-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0093-5006-98 [00093500698]

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202491
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-11-14
Marketing End Date2018-06-30

NDC 0093-5006-56 [00093500656]

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202491
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-11-14

Drug Details

Active Ingredients

IngredientStrength
OLMESARTAN MEDOXOMIL40 mg/1

OpenFDA Data

SPL SET ID:5c128ef2-60a6-40f3-b37f-ee139fe27987
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 999991
  • 999996
  • 999986
  • 1000001
  • 999967
  • UPC Code
  • 0300935006987
  • 0300935004983
  • 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]

    NDC Crossover Matching brand name "Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide" or generic name "Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0093-5002Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    0093-5003Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    0093-5004Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    0093-5005Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    0093-5006Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    53808-1120Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazideolmesartan medoxomil, amlodipine besylate and hydrochlorothiazide
    57664-796Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazideolmesartan medoxomil, amlodipine besylate and hydrochlorothiazide
    57664-797Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazideolmesartan medoxomil, amlodipine besylate and hydrochlorothiazide
    70518-1648Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    57664-800Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    57664-798Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
    57664-799Olmesartan Medoxomil, Amlodipine and HydrochlorothiazideOlmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

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