NDC 42708-204
Amlodipine Besylate 5 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-901.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
| Alkem Laboratories Limited | Baddi Solan, India | Makes it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Amlodipine: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078925
- On the market since
- Dec 6, 2025
- Package NDCs
42708-204-30- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?