NDC 71205-320
Benazepril Hydrochloride 40 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
71205-320-3071205-320-6071205-320-90- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2019
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