NDC 68180-101
Valsartan and Hydrochlorothiazide 320 mg / 12.5 mg tablet, film coated
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrochlorothiazide and Valsartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 320 mg / 12.5 mg
- Approval
- ANDA ANDA078946
- On the market since
- Mar 21, 2013
- Package NDCs
68180-101-0268180-101-0968180-101-11- Official label
- DailyMed (National Library of Medicine), updated Nov 30, 2023
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