Olmesartan Medoxomil And Hydrochlorothiazide 67877-0452
Product NDC
67877-0452- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA207037
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 12.5 mg/1 |
| Olmesartan Medoxomil | 40 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (67877-452-30)
90 TABLET, FILM COATED in 1 BOTTLE (67877-452-90)