Benazepril Hydrochloride 62135-0721
Product NDC
62135-0721- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 20, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA076267
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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)
90 TABLET in 1 BOTTLE (62135-721-90)