NDC 67296-1682

Hydrochlorothiazide 25 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-397.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Generics Bidco II LLC d/b/a Prinston LaboratoriesCharlotte, NC, United StatesMakes it Problems found, fixed voluntarilySep 19, 2025 · 10 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet
Strength
25 mg
Approval
ANDA ANDA040412
On the market since
Jan 1, 2019
Package NDCs
67296-1682-3
Official label
DailyMed (National Library of Medicine), updated Aug 3, 2024

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