NDC 51655-388
Benazepril Hydrochloride 20 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Aurobindo Pharma Limited's NDC 65862-117.
Where the pills inside were 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 |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
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
- May 19, 2023
- Package NDCs
51655-388-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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