Where it's 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
- Dec 22, 2017
- Package NDCs
10702-201-0110702-201-1010702-201-50- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?