NDC 0440-5000

Alfuzosin hydrochloride 10 mg tablet, extended release

On the label: Liberty Pharmaceuticals, Inc.. It's repackaged: Liberty Pharmaceuticals, Inc. rebottles it from Exelan Pharmaceuticals, Inc.'s NDC 76282-302.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
InvaGen Pharmaceuticals, IncHauppauge, NY, United StatesMakes it and tests it No problems foundOct 25, 2023 · 18 inspections
InvaGen Pharmaceuticals, IncCentral Islip, NY, United StatesTests it and packages it Problems found, fixed voluntarilyJul 17, 2026 · 4 inspections

Product details

Generic drug
Alfuzosin: every company that makes it
Form
tablet, extended release
Strength
10 mg
Approval
ANDA ANDA090284
On the market since
Oct 2, 2012
Package NDCs
0440-5000-90
Official label
DailyMed (National Library of Medicine), updated Aug 9, 2016

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