NDC 51655-272

Hydrochlorothiazide 25 mg tablet

On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-008.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.East Brunswick, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundSep 19, 2023 · 10 inspections

Repackaging site

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
25 mg
Approval
ANDA ANDA085182
On the market since
May 4, 2020
Package NDCs
51655-272-26 51655-272-52
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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