NDC 54458-863
Benazepril Hydrochloride 20 mg tablet, coated
On the label: International Laboratories, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zhejiang Huahai Pharmaceutical Co., Ltd. | Linhai, China | Makes it | Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action |
Product details
- Generic drug
- Benazeprilat: every company that makes it
- Form
- tablet, coated
- Strength
- 20 mg
- Approval
- ANDA ANDA076118
- On the market since
- Feb 1, 2014
- Package NDCs
54458-863-1054458-863-16- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2019
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