NDC 72789-412
Amlodipine and Benazepril Hydrochloride 10 mg / 20 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. 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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, 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
- Sep 5, 2012
- Package NDCs
72789-412-90- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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