NDC 67296-2045
Oxybutynin Chloride 5 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Leading Pharma, LLC's NDC 69315-182.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| LIFEPharma FZE | Dubai, United Arab Emirates | Makes it and tests it | Problems found, fixed voluntarilyNov 24, 2022 · 1 inspection |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA212798
- On the market since
- Nov 1, 2019
- Package NDCs
67296-2045-3- Official label
- DailyMed (National Library of Medicine), updated Jan 23, 2025
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