NDC 72319-006

Selegiline Hydrochloride 5 mg tablet

On the label: i3 Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
i3 Pharmaceuticals, LLCWarminster, PA, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 22, 2026 · 4 inspections

Product details

Generic drug
Selegiline: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA074672
On the market since
Dec 15, 2021
Package NDCs
72319-006-02
Official label
DailyMed (National Library of Medicine), updated Mar 20, 2024

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