NDC 72789-417
Oxybutynin Chloride 5 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-431.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA209025
- On the market since
- Feb 1, 2018
- Package NDCs
72789-417-3072789-417-90- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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