NDC 67877-453 – Olmesartan Medoxomil And Hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-453
Product details
- Brand name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207037
- Marketed since
- May 1, 2025
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 67877-453-30 | 30 TABLET, FILM COATED in 1 BOTTLE (67877-453-30) | May 1, 2025 |
| 67877-453-90 | 90 TABLET, FILM COATED in 1 BOTTLE (67877-453-90) | May 1, 2025 |
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