NDC 68788-8454
Amlodipine and Benazepril Hydrochloride 10 mg / 20 mg capsule
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred 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
- Preferred Pharmaceuticals Inc., Anaheim, CA, 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
- Jun 2, 2023
- Package NDCs
68788-8454-3- Official label
- DailyMed (National Library of Medicine), updated Feb 27, 2026
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