NDC 83008-086

Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet, film coated

On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged: Lake Erie Medical DBA Quality Care Products LLC rebottles it from Solco Healthcare U.S., LLC's NDC 43547-424.

China: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zhejiang Huahai Pharmaceutical Co., Ltd.Linhai, ChinaMakes it Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action
Zhejiang Huahai Pharmaceutical Technology Co., Ltd.Taizhou, ChinaMakes it Problems found, fixed voluntarilyAug 22, 2025 · 1 inspection

Repackaging site

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
Aug 28, 2024
Package NDCs
83008-086-90
Official label
DailyMed (National Library of Medicine), updated Dec 19, 2024

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