NDC 72789-414
Oxybutynin ChlorideExtended Release 10 mg tablet, extended release
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-210.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it | Problems found, fixed voluntarilyOct 23, 2022 · 6 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 ANDA206121
- On the market since
- Sep 27, 2016
- Package NDCs
72789-414-90- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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