NDC 70756-812 – Olmesartan Medoxomil and Hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC70756-812
Product details
- Brand name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Labeler
- Lifestar Pharma LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208847
- Marketed since
- October 1, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70756-812-12 | 1000 TABLET in 1 BOTTLE (70756-812-12) | Oct 1, 2020 |
| 70756-812-30 | 30 TABLET in 1 BOTTLE (70756-812-30) | Oct 1, 2020 |
| 70756-812-51 | 500 TABLET in 1 BOTTLE (70756-812-51) | Oct 1, 2020 |
| 70756-812-90 | 90 TABLET in 1 BOTTLE (70756-812-90) | Oct 1, 2020 |
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