NDC 68071-4722
Benazepril Hydrochloride 40 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- NuCare Pharmaceuticals,Inc., Orange, CA, 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
68071-4722-9- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?