NDC 53002-1804
Amlodipine and Benazepril Hydrochloride 10 mg / 40 mg capsule
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-587.
Where the pills inside were 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 |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Amlodipine and Benazeprilat: every company that makes it
- Form
- capsule
- Strength
- 10 mg / 40 mg
- Approval
- ANDA ANDA202239
- On the market since
- Sep 5, 2012
- Package NDCs
53002-1804-0- Official label
- DailyMed (National Library of Medicine), updated Nov 23, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?