NDC 69367-219

Hydrochlorothiazide 12.5 mg capsule

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
capsule, oral
Strength
12.5 mg
Approval
ANDA ANDA203561
On the market since
Jun 7, 2019
Package NDCs
69367-219-01 69367-219-05 69367-219-10
Official label
DailyMed (National Library of Medicine), updated Sep 29, 2026

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