Benazepril Hydrochloride 50268-0111
Product NDC
50268-0111- Manufacturer
- Avpak
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 28, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA076820
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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(1)
50 BLISTER PACK in 1 BOX (50268-111-15) / 1 TABLET in 1 BLISTER PACK (50268-111-11)