NDC 70518-3420
Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-424.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zhejiang Huahai Pharmaceutical Co., Ltd. | Linhai, China | Makes it | Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action |
| Zhejiang Huahai Pharmaceutical Technology Co., Ltd. | Taizhou, China | Makes it | Problems found, fixed voluntarilyAug 22, 2025 · 1 inspection |
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg / 100 mg
- Approval
- ANDA ANDA204901
- On the market since
- May 16, 2022
- Package NDCs
70518-3420-070518-3420-170518-3420-270518-3420-370518-3420-4- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?