NDC 66993-345
Lofexidine hydrochloride 0.2 mg tablet, film coated
On the label: Prasco Laboratories.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Catalent Pharma Solutions, LLC | Winchester, KY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 22, 2025 · 10 inspections |
| A+ Secure Packaging, LLC | La Vergne, TN, United States | Packages it and labels it | No problems foundJun 7, 2023 · 4 inspections |
| Acceleration Laboratory Services Inc. | Lee's Summit, MO, United States | Tests it | Problems found, fixed voluntarilyJul 11, 2024 · 4 inspections |
| UFAG Laboratorien AG | Sursee, Switzerland | Tests it | No problems foundMar 14, 2023 · 4 inspections |
Product details
- Generic drug
- Lofexidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 0.2 mg
- Approval
- NDA authorized generic NDA209229
- On the market since
- Aug 29, 2024
- Package NDCs
66993-345-3766993-345-76- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?