NDC 43547-391 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC43547-391
Product details
- Brand name
- OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- Generic name
- Olmesartan medoxomil and hydrochlorothiazide
- Labeler
- Solco Healthcare US, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207804
- Marketed since
- April 24, 2017
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 43547-391-03 | 30 TABLET in 1 BOTTLE (43547-391-03) | Apr 24, 2017 |
| 43547-391-09 | 90 TABLET in 1 BOTTLE (43547-391-09) | Apr 24, 2017 |
| 43547-391-11 | 1000 TABLET in 1 BOTTLE (43547-391-11) | Apr 24, 2017 |
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