NDC 53002-1785
Valsartan and Hydrochlorothiazide 25 mg / 160 mg tablet, film coated
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-105.
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
- RPK Pharmaceuticals, Inc., Union City, 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 / 160 mg
- Approval
- ANDA ANDA078946
- On the market since
- Mar 21, 2013
- Package NDCs
53002-1785-353002-1785-9- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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