Olmesartan Medoxomil And Hydrochlorothiazide 31722-0888
Product NDC
31722-0888- Manufacturer
- Camber Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 25, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA209199
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Olmesartan Medoxomil | 40 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (31722-888-30)
10 BLISTER PACK in 1 CARTON (31722-888-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
90 TABLET, FILM COATED in 1 BOTTLE (31722-888-90)