NDC 71335-2180 – Olmesartan Medoxomil and Hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC71335-2180
Product details
- Brand name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208847
- Marketed since
- October 1, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 40 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2180-1 | 30 TABLET in 1 BOTTLE (71335-2180-1) | Oct 13, 2022 |
| 71335-2180-2 | 90 TABLET in 1 BOTTLE (71335-2180-2) | Oct 13, 2022 |
| 71335-2180-3 | 28 TABLET in 1 BOTTLE (71335-2180-3) | Jan 31, 2025 |
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