NDC 69584-362

Hydrochlorothiazide 50 mg tablet

On the label: Oxford Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA087068
On the market since
Sep 25, 2020
Package NDCs
69584-362-10 69584-362-90
Official label
DailyMed (National Library of Medicine), updated Aug 18, 2025

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