Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Corium Innovations, Inc. | Grand Rapids, MI, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyNov 18, 2022 · 7 inspections |
| Eurofins Lancaster Laboratories, LLC | Lancaster, PA, United States | Tests it | Problems found, fixed voluntarilyAug 26, 2025 · 8 inspections |
Recalls
- Jun 9, 2022 · Class II · Mayne Pharma Inc
Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
Lots: Lot: 41179A Exp. Jan 2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Clonidine: every company that makes it
- Form
- patch, extended release
- Strength
- 0.1 mg per 24 h
- Approval
- ANDA ANDA079090
- On the market since
- Aug 3, 2016
- Package NDCs
51862-453-0151862-453-04- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?