NDC 65862-133

Hydrochlorothiazide 25 mg tablet

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
25 mg
Approval
ANDA ANDA040780
On the market since
Jul 20, 2007
Package NDCs
65862-133-01 65862-133-99
Official label
DailyMed (National Library of Medicine), updated Jun 26, 2024

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