NDC 70518-2640
Oxybutynin Chloride 5 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-201.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Recalls
- Dec 11, 2018 · Class II · KVK-Tech, Inc.
Labeling: Wrong bar code
Lots: Lot #: 15079A, Exp 10/20
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA209335
- On the market since
- Mar 26, 2020
- Package NDCs
70518-2640-070518-2640-170518-2640-270518-2640-370518-2640-4- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2026
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