NDC 57237-144
Amlodipine and Benazepril Hydrochloride 5 mg / 20 mg capsule
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Amlodipine and Benazeprilat: every company that makes it
- Form
- capsule, oral
- Strength
- 5 mg / 20 mg
- Approval
- ANDA ANDA202239
- On the market since
- Sep 5, 2012
- Package NDCs
57237-144-0157237-144-05- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2024
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