NDC 84386-101
Benazepril Hydrochloride 20 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Benazeprilat: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078212
- On the market since
- Jan 13, 2026
- Package NDCs
84386-101-0184386-101-90- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
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