NDC 82804-239
Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Solco Healthcare U.S., LLC's NDC 43547-423.
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 |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg / 12.5 mg
- Approval
- ANDA ANDA204901
- On the market since
- Feb 15, 2018
- Package NDCs
82804-239-30- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2025
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