0093-5005 : Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated


NDC: 0093-5005
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name: Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA202491
Rev. Date: 


Appearance:


Markings: TEVA;5005
Shapes:  Round
Colors:  Pink
Size (mm): 8
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 0093-5005-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑5005‑56)
  • 0093-5005-98: 90 TABLET, FILM COATED IN 1 BOTTLE (0093‑5005‑98)

Active Ingredients:

  • Olmesartan Medoxomil
  • Amlodipine Besylate
  • Hydrochlorothiazide

Dosage Strength:

  • 20 mg
  • 5 mg
  • 12.5 mg

Inactive Ingredients:

  • Crospovidone (12 Mpa.s At 5%)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Polyethylene Glycol 3350
  • Polyvinyl Alcohol, Unspecified
  • Povidone K30
  • Silicon Dioxide
  • Sodium Starch Glycolate Type a Potato
  • Talc
  • Titanium Dioxide
  • Fd&c Red No. 40
  • Ferrosoferric Oxide
  • Ferric Oxide Yellow

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0093-5002 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-5003 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-5004 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 0093-5006 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
  • 53808-1120 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Doh Central Pharmacy
  • 57664-796 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 57664-797 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 57664-798 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 57664-799 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 57664-800 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Sun Pharmaceutical Industries, Inc.
  • 70518-1648 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Oral Tablet, Film Coated by Remedyrepack Inc.

NDC QR Code

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NDC 0093-5005 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.