NDC 70954-909

Lofexidine 0.18 mg tablet

On the label: ANI Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Product details

Generic drug
Lofexidine: every company that makes it
Form
tablet, oral
Strength
0.18 mg
Approval
ANDA ANDA219917
On the market since
Oct 22, 2025
Package NDCs
70954-909-10 70954-909-20
Official label
DailyMed (National Library of Medicine), updated Sep 5, 2024

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