Benazepril Hydrochloride 71335-0078
Product NDC
71335-0078- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA076118
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benazepril Hydrochloride | 20 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]
Packaging Options(6)
30 TABLET, COATED in 1 BOTTLE (71335-0078-1)
60 TABLET, COATED in 1 BOTTLE (71335-0078-2)
100 TABLET, COATED in 1 BOTTLE (71335-0078-3)
90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
10 TABLET, COATED in 1 BOTTLE (71335-0078-6)