NDC 70518-3780

Hydrochlorothiazide 50 mg tablet

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-009.

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

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA085182
On the market since
Jul 9, 2023
Package NDCs
70518-3780-0 70518-3780-1
Official label
DailyMed (National Library of Medicine), updated May 7, 2025

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