NDC 68258-6969
Valsartan and Hydrochlorothiazide 25 mg / 320 mg tablet, film coated
On the label: Dispensing Solutions Inc.. It's repackaged: Dispensing Solutions Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-102.
Where the pills inside were 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 |
Repackaging site
- Dispensing Solutions Inc., Santa Ana, California, United States · repackages it and relabels it
Product details
- Generic drug
- Hydrochlorothiazide and Valsartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 25 mg / 320 mg
- Approval
- ANDA ANDA078946
- On the market since
- Mar 21, 2013
- Package NDCs
68258-6969-9- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?