NDC 51655-213
Amlodipine and Benazepril Hydrochloride 10 mg / 20 mg capsule
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Aurobindo Pharma Limited's NDC 65862-586.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Amlodipine and Benazeprilat: every company that makes it
- Form
- capsule, oral
- Strength
- 10 mg / 20 mg
- Approval
- ANDA ANDA202239
- On the market since
- Oct 20, 2022
- Package NDCs
51655-213-2651655-213-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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