NDC 71921-250
Lofexidine 0.18 mg tablet, coated
On the label: Florida Pharmaceutical Products, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Indoco Remedies Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJan 20, 2023 · 3 inspections, 1 with FDA action |
Product details
- Generic drug
- Lofexidine: every company that makes it
- Form
- tablet, coated, oral
- Strength
- 0.18 mg
- Approval
- ANDA ANDA218613
- On the market since
- Aug 21, 2024
- Package NDCs
71921-250-3671921-250-96- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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