NDC 50228-112

Hydrochlorothiazide 50 mg tablet

On the label: ScieGen Pharmaceuticals, Inc..

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
tablet, oral
Strength
50 mg
Approval
ANDA ANDA203018
On the market since
Feb 5, 2014
Package NDCs
50228-112-10 50228-112-30
Official label
DailyMed (National Library of Medicine), updated May 11, 2020

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