NDC 43386-712

Quinapril HCL and Hydrochlorothiazide 20 mg / 25 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Hydrochlorothiazide and Quinaprilat: every company that makes it
Form
tablet, oral
Strength
20 mg / 25 mg
Approval
ANDA ANDA076374
On the market since
Jul 15, 2011
Package NDCs
43386-712-03 43386-712-05 43386-712-09
Official label
DailyMed (National Library of Medicine), updated Jan 30, 2024

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