NDC 63304-156
Benazepril hydrochloride and hydrochlorothiazide 20 mg / 12.5 mg tablet, 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 |
Product details
- Generic drug
- Benazeprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, coated
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA077483
- On the market since
- Apr 10, 2006
- Package NDCs
63304-156-0163304-156-1063304-156-30- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2015
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