NDC 24208-314
Flurbiprofen Sodium 0.3 mg per 1 mL solution/ drops
On the label: Bausch & Lomb Incorporated.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch & Lomb Incorporated | Tampa, FL, United States | Makes it | Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action |
Product details
- Generic drug
- Flurbiprofen: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 0.3 mg per 1 mL
- Approval
- ANDA ANDA074447
- On the market since
- Jan 4, 1995
- Package NDCs
24208-314-25- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?