NDC 68788-7790

Hydrochlorothiazide 50 mg tablet

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, 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

Repackaging site

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA085182
On the market since
Oct 21, 2020
Package NDCs
68788-7790-0 68788-7790-1 68788-7790-3 68788-7790-6 68788-7790-9
Official label
DailyMed (National Library of Medicine), updated May 11, 2026

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