NDC 63304-738
Benazepril Hydrochloride 20 mg tablet, film coated
On the label: Ranbaxy Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ohm Laboratories Inc. | North Brunswick, NJ, United States | Makes it | No problems foundOct 31, 2024 · 22 inspections |
| Ranbaxy laboratories Limited Toansa | Location not on file | Makes the active ingredient | Not inspected on record |
Product details
- Generic drug
- Benazeprilat: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA076344
- On the market since
- Feb 11, 2004
- Package NDCs
63304-738-1063304-738-3063304-738-77- Official label
- DailyMed (National Library of Medicine), updated Apr 29, 2015
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