NDC 50090-3561 – Olmesartan Medoxomil and Hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-3561
Product details
- Brand name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205391
- 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 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50090-3561-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3561-0) | Aug 30, 2018 |
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