NDC 53217-335
Oxybutynin Chloride 5 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-0038.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Repackaging site
- Aidarex Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA074625
- On the market since
- Oct 5, 2017
- Package NDCs
53217-335-30- Official label
- DailyMed (National Library of Medicine), updated Aug 13, 2018
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