NDC 69315-155

Hydrochlorothiazide 12.5 mg tablet

On the label: Leading Pharma, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Leading Pharma, LLCFairfield, NJ, United StatesMakes it Problems found, fixed voluntarilyOct 21, 2024 · 13 inspections

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
12.5 mg
Approval
ANDA ANDA040702
On the market since
Nov 1, 2019
Package NDCs
69315-155-01 69315-155-10
Official label
DailyMed (National Library of Medicine), updated Jun 12, 2026

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