NDC 53808-0873

Oxybutynin Chloride 5 mg tablet

On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-0038.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it and tests it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Repackaging site

Product details

Generic drug
Oxybutynin: every company that makes it
Form
tablet
Strength
5 mg
Approval
ANDA ANDA074625
On the market since
Jan 1, 2013
Package NDCs
53808-0873-2
Official label
DailyMed (National Library of Medicine), updated Sep 26, 2013

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