NDC 46708-151 – Olmesartan Medoxomil and Hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC46708-151
Product details
- Brand name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204233
- Marketed since
- April 24, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 40 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 46708-151-08 | 80 TABLET in 1 CARTON (46708-151-08) | Apr 24, 2017 |
| 46708-151-10 | 100 TABLET in 1 CARTON (46708-151-10) | Apr 24, 2017 |
| 46708-151-30 | 30 TABLET in 1 BOTTLE (46708-151-30) | Apr 24, 2017 |
| 46708-151-90 | 90 TABLET in 1 BOTTLE (46708-151-90) | Apr 24, 2017 |
| 46708-151-91 | 1000 TABLET in 1 BOTTLE (46708-151-91) | Apr 24, 2017 |
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