70518-2647 : Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/5/25 mg Oral Tablet


NDC: 70518-2647
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/5/25 mg
Dosage Form: Oral Tablet
Application #: ANDA203580
Rev. Date: 


Appearance:


Shapes:  Oval
Colors:  Yellow
Size (mm): 11
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:

  • 70518-2647-0: 30 TABLET IN 1 BOTTLE, PLASTIC (70518‑2647‑0)

Active Ingredients:

  • Olmesartan Medoxomil
  • Amlodipine
  • Hydrochlorothiazide

Dosage Strength:

  • 40 mg
  • 5 mg
  • 25 mg

Inactive Ingredients:

  • Croscarmellose Sodium
  • Silicon Dioxide
  • Magnesium Stearate
  • Talc
  • Lactose Monohydrate
  • Starch, Corn
  • Polyvinyl Alcohol, Unspecified
  • Smcc
  • Titanium Dioxide
  • Ferric Oxide Yellow
  • Polyethylene Glycol 400 /

Pharmaceutical Classes:

  • 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]

Related Products:

Based on records with the same trade name.
  • 13668-385 Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 40/5/25 mg Oral Tablet by Torrent Pharmaceuticals Limited

NDC QR Code

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NDC 70518-2647 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.