Benazepril Hydrochloride And Hydrochlorothiazide 72888-0222
Product NDC
72888-0222- Manufacturer
- Advagen Pharma Ltd
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2024
- Listing Expires
- December 31, 2027
- Application
- NDA020033
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 20 mg/1 |
| Hydrochlorothiazide | 25 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(1)
100 TABLET in 1 BOTTLE (72888-222-01)