NDC 65862-835
Amlodipine, Valsartan and Hydrochlorothiazide 5 mg / 25 mg / 160 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
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 Hydrochlorothiazide and Valsartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg / 25 mg / 160 mg
- Approval
- ANDA ANDA206180
- On the market since
- Dec 19, 2017
- Package NDCs
65862-835-0565862-835-3065862-835-90- Official label
- DailyMed (National Library of Medicine), updated May 17, 2024
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