NDC 72205-246
lofexidine hydrochloride 0.2 mg tablet, film coated
On the label: Novadoz Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| MSN Laboratories Private Limited | Rangareddy District, India | Makes it and tests it | Problems found, fixed voluntarilyDec 21, 2023 · 4 inspections |
Product details
- Generic drug
- Lofexidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 0.2 mg
- Approval
- ANDA ANDA218699
- On the market since
- Feb 24, 2025
- Package NDCs
72205-246-4272205-246-43- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2024
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