NDC 43063-748
Benazepril Hydrochloride 40 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-118.
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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Benazeprilat: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA078212
- On the market since
- May 22, 2008
- Package NDCs
43063-748-30- Official label
- DailyMed (National Library of Medicine), updated May 14, 2026
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