NDC 72789-049
oxybutynin chloride 10 mg tablet, extended release
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Accord Healthcare Inc.'s NDC 16729-318.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Intas Pharmaceuticals Limited | Ahmedabad, India | Makes it and tests it | No problems foundJul 12, 2024 · 10 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, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA207138
- On the market since
- Dec 20, 2016
- Package NDCs
72789-049-90- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2026
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