NDC 81033-109
Valsartan 320 mg tablet, film coated
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Ascend Laboratories, LLC's NDC 67877-418.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · labels it and repackages it
Product details
- Generic drug
- Valsartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 320 mg
- Approval
- ANDA ANDA205536
- On the market since
- Mar 14, 2019
- Package NDCs
81033-109-3181033-109-32- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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