NDC 52817-261

Oxybutynin Chloride 2.5 mg tablet

On the label: TruPharma LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Tulex Pharmaceuticals IncCranbury, NJ, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMar 24, 2025 · 4 inspections

Product details

Generic drug
Oxybutynin: every company that makes it
Form
tablet, oral
Strength
2.5 mg
Approval
ANDA ANDA210125
On the market since
Jul 28, 2026
Package NDCs
52817-261-10
Official label
DailyMed (National Library of Medicine), updated Jul 27, 2026

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