71335-0775 : Olmesartan Medoxomil 20 mg Oral Tablet, Film Coated


NDC: 71335-0775
Labeler: Bryant Ranch Prepack
Product Type: Human Prescription Drug
Drug Name: Olmesartan Medoxomil
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA207662
Rev. Date: 


Appearance:


Markings: FS2
Shapes:  Round
Colors:  White
Size (mm): 9
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:

  • 71335-0775-1: 30 TABLET, FILM COATED IN 1 BOTTLE (71335‑0775‑1)
  • 71335-0775-2: 60 TABLET, FILM COATED IN 1 BOTTLE (71335‑0775‑2)
  • 71335-0775-3: 90 TABLET, FILM COATED IN 1 BOTTLE (71335‑0775‑3)
  • 71335-0775-4: 180 TABLET, FILM COATED IN 1 BOTTLE (71335‑0775‑4)

Active Ingredients:

  • Olmesartan Medoxomil

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Hypromellose, Unspecified
  • Lactose Monohydrate
  • Low-substituted Hydroxypropyl Cellulose, Unspecified
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Talc
  • Titanium Dioxide /

Pharmaceutical Classes:

  • Angiotensin 2 Receptor Antagonists [MoA]
  • Angiotensin 2 Receptor Blocker [EPC]

Related Products:

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  • 63629-8524 Olmesartan Medoxomil 40 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
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NDC QR Code

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NDC 71335-0775 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.