NDC 50090-4622
Oxybutynin Chloride 5 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions 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 |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
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
- Dec 22, 2017
- Package NDCs
50090-4622-050090-4622-150090-4622-3- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2024
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