Benazepril Hydrochloride 65162-0751
Product NDC
65162-0751- Manufacturer
- Amneal Pharmaceuticals Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 2, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA076820
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 5 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(3)
30 TABLET in 1 BOTTLE (65162-751-03)
100 TABLET in 1 BOTTLE (65162-751-10)
500 TABLET in 1 BOTTLE (65162-751-50)