71335-2448 : Olmesartan Medoxomil 20 mg Oral Tablet, Coated
NDC: | 71335-2448 |
Labeler: | Bryant Ranch Prepack |
Product Type: | Human Prescription Drug |
Drug Name: | Olmesartan Medoxomil |
Dosage Form: | Oral Tablet, Coated |
Application #: | ANDA206763 |
Rev. Date: |
NDC Package Codes:
- 71335-2448-1: 30 TABLET, COATED IN 1 BOTTLE (71335‑2448‑1)
- 71335-2448-2: 60 TABLET, COATED IN 1 BOTTLE (71335‑2448‑2)
- 71335-2448-3: 90 TABLET, COATED IN 1 BOTTLE (71335‑2448‑3)
- 71335-2448-4: 180 TABLET, COATED IN 1 BOTTLE (71335‑2448‑4)
Active Ingredients:
- Olmesartan Medoxomil
Dosage Strength:
- 20 mg
Pharmaceutical Classes:
- Angiotensin 2 Receptor Antagonists [MoA]
- Angiotensin 2 Receptor Blocker [EPC]
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- 63629-8523 Olmesartan Medoxomil 20 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
- 63629-8524 Olmesartan Medoxomil 40 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
- 63629-8525 Olmesartan Medoxomil 40 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
- 63629-9426 Olmesartan Medoxomil 5 mg Oral Tablet, Film Coated by Bryant Ranch Prepack
- 0093-7610 Olmesartan Medoxomil 5 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
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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.